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00:12 what? Mhm. No. Well would be. Yeah. Okay.

00:46 . Uh Let's get started. Let's . So um Today we're going to

01:00 chapter 24 On the data immune Talk a little bit about vaccines in

01:08 . And then um Thursday it's chapter . So it's kind of like that

01:15 , so not a bunch of And around the different topics coming to

01:23 check pretty fine. It's microbial. we'll talk about that and then uh

01:30 see the next week, is So wrap it up with different

01:34 So I'll mention I'll talk about that the third day. Um Smart work

01:40 doing is deeply quiz this week. Exam three. So you can look

01:46 that tomorrow, it will be up across uh and look at it the

01:52 the schedule for the last exam should 26. I haven't seen it officially

02:01 in a calendar in uh courseware, that's that's the 26th, two weeks

02:08 the baby's aunt that normally wouldn't help . So uh but anyway, so

02:14 let's keep an eye out on Um And so in terms of the

02:19 three, the overall it's fun over Average seven nearly 72. Um half

02:31 median. So certainly certainly uh more higher on this side. Uh good

02:42 . Um so anyway, so um you know the so do take a

02:49 at it when it's available questions. me know. Um But you know

02:53 this point just having amnesia. Pretty good. Not so good somewhere

03:00 the middle. Just have magnesia, all energies on the last opportunity to

03:07 , right. Which are which are to quiz is still a couple of

03:12 to do. Uh Then then the example. Okay. And uh they're

03:21 this is still almost almost a month the last exam. So Three weeks

03:27 generally more or less. And so plenty of time I will stand

03:32 It's up to 34 besides this. uh if you have questions, I'll

03:37 available throughout the financial security. if you want to take a meeting

03:41 what have you? Not a So, but just let me know

03:46 of time that won't that that will will be a problem. So,

03:51 Okay, so uh what else we um any questions about anything you

04:01 Okay. All right. Um So let's we're gonna start with a

04:07 . Okay. So this is kind I'm gonna we'll start with a little

04:10 of a recap and stuff from last . It was kind of meant to

04:13 a little bit of that and then other things we don't talk about all

04:17 things last time. Uh but we're get into more of the uh the

04:25 of the adaptive immune system um that that you have of that and how

04:31 operate. Uh So let's just kind see how we do here. So

04:42 you're looking at this. So you a look at some of the

04:45 Your book doesn't have an extensive section the vaccine. Some of the stuff

04:49 talked about there is really from the I use for the pre nursing

04:55 Um But not not meant to be great detail was kind of present.

05:00 you know, here's here's different types vaccines to use a little bit about

05:06 Covid vaccines. Um And so it's just like here's a survey of different

05:12 and a little bit more in depth a couple of them. But but

05:18 just kind of barrel knowledge type. dr was a Turning Point website.

05:28 don't know how is it different? working. That's insane. Alright.

05:34 hold on, let me uh the is working. But what's not

05:41 The when you go on. Oh , I honestly can't tell you.

05:47 uh All we can do on my is a cure. I mean if

05:53 have the mobile app, you're seeing usual thing, right? Which you

05:57 see on the on the mobile You're seeing the normal, everything's

06:02 Okay. Mhm. Hold on. Let's see more responses. That's

06:14 Right? Um That's still weird. . Work. Work. Okay.

06:21 . Um assume assume. Uh this is Okay. Issues. All

06:31 , Okay. Um Alright. So let's let's move on here. So

06:37 see what we got here. just around the booth. They're moving

06:42 again. Okay. Looks like uh let's let's just go through these.

06:48 what's the false one. So the mostly immediate human oral t cells most

06:53 sale. That's that's true. That's the that's just the definition there.

06:58 . Um B cells can differentiate into secreting plasma cells. That's true.

07:04 also into memory cells. Uh T can directly kill infected host cells.

07:12 can sort of toxic T cells can that. B cells do not they

07:18 directly kill cells. They work through . Right? So they can they

07:22 produce antibody that can interact with a but they don't really kill directly.

07:28 , so that's true. So this is single clonal population of plasma cells

07:37 and bodies to many different episodes. it's kind of that's the key word

07:43 . Colonial population. So they would colonial population will produce antibodies to the

07:50 appetite. Okay, that's what Colin has. We'll talk about that

07:55 And these B cell function. So have multiple sets of B cells in

08:02 body. And each cool. Or of B cells can respond to particular

08:10 . Okay. And then the one does only that population will then proliferate

08:17 antibodies but almost any bodies you will specific for that one at the

08:23 Okay, so this this is false written. It would be antibodies to

08:28 single and the talent. Okay. make that interesting. Only still

08:35 I'm sorry. Okay. Yes. we go doctor clothes. That's

08:45 It doesn't matter. It doesn't It's um it's fine. Um

08:55 Any questions so we're going to elaborate these points as we go through.

09:00 . Um okay. So we talked this last time. Everybody at that

09:07 to have kind of the features of and so elaborate on that.

09:13 We did talk about more on the of antibodies and binding. So the

09:20 episodes remember that the is the larger smaller important in the larger Anthony and

09:29 occurs on the episode between it and and body. Okay. Um and

09:37 of the angel's can be a variety things. Okay, there are many

09:41 that can be on the periphery of virus or bacteria or protozoan and whatever

09:47 and type is, which can be bunch of different things that challenge capsule

09:54 on the surface of different types Okay. Um so so cleverly division

10:01 is after cellular pathogens interest. And these cells respond to these antibodies that

10:08 work on extra sailings. Uh so talking t cells interact with infected

10:17 Do you help yourselves? Different types Iraq with the arrangement clinic cells b

10:22 etcetera more elaborate on that today. . So um when we talk about

10:29 terminology structure. So remembering this y structure um you can define new

10:39 So you have five IHSA types and and video type uh within a nice

10:49 type. So you have a ice type. For example within that Dyson

10:54 you can have multiple media types. ? And so we can define an

10:59 . G. A. By the in uh sequence of the peptides in

11:07 constant regions. Okay so all I . H. Will be the same

11:12 that area. All I G. . Will be the same. Alright

11:17 but then of course we have differences you can certainly have A G.

11:22 . That will bind it's an But you also advised us that will

11:25 different engines. Okay. Um and the EEA type Aisa type difference.

11:33 um and then uh the effects of engine mining. Okay so organization in

11:44 nation and clumping reaction neutralization uh coding viruses, bacteria antibody will prevent them

11:51 binding to sell. Uh compliment. dependent. So mediated toxicity way too

12:02 . Um And so kind of reserved bringing down large multi sale.

12:10 To do something like this takes a effort in a way to bring music

12:15 together is through an inbox. And the sites. Remember you're gonna have

12:21 just an engine binding sites out of . Okay but also binding site here

12:27 that's where various cell types combined. it's for something like optimization.

12:33 Um or this response. Okay so like using the phones will will congregate

12:41 my antibody and then release toxins that the parasite. Okay so um so

12:49 can now then look a little bit different types of hand body classes.

12:55 so remember that I. G. . Stands for just another fancy term

12:59 antibody. Okay so um so D. A. S. Are

13:06 in um preventing potential pathogens from the to your services specifically from social

13:15 So remember your mucosa is one of . It's a physical barrier.

13:19 Also chemical barrier is mucus which can different types of criminals in it including

13:27 . D. A. Okay and many of your respiratory pathogens um rely

13:35 the here to yourselves of your respiratory which of course is farming forestry services

13:43 I. G. A. Their those pathogens can prevent combined and then

13:48 them from buying. Okay certainly. their ability to call it disease.

13:52 so um the and this algerians type informal diet like this so basically increasing

14:01 number of and combining sites. So ounce four for three. Okay so

14:09 uh so the percentages again are what presence are in abundance and blood circulating

14:14 . So relatively low mostly in the . Bye. Um So then

14:22 G. Um G. Is probably of the more workforce types of antibodies

14:30 call it. They made their functions you see here higher concentration blood.

14:37 highest of the five classes in terms blood concentration involved multiple functions neutralizing antibody

14:46 . The optimization Activate complement. So it is the one when you get

14:54 or if you have an infection G. M's are generally the first

14:59 that come out but then they followed by I. G. And

15:04 G. Tend to be more stronger and more active than say okay um

15:13 I. G. D. So gonna have and body types that I

15:17 either function alone just kind of float but rather they sit on top of

15:22 cell. Okay. And so the interactive engine one way is through uh

15:30 on their surface. Okay so the Tootie's and bodies will activate and get

15:36 evacuate. Okay. Um And so because details are primarily found pathetic food

15:45 I. D. D. And him to be where they're at.

15:48 I'm not gonna be a high concentrations the blood for them. Okay um

15:53 here would be a is it pathogen and creating effect? Okay.

16:02 So as mentioned these are kind of first antibodies on the scene uh in

16:07 possible infection. Um They have a uh forming these. Lawrence performs okay

16:16 remember that the illumination function uh pathogens infectious units if you will. And

16:24 lumping them together and now you reduce numbers so now you effectively bring it

16:29 to fewer units to deal with. so uh because they have five of

16:36 together breaking out 10 10 binding So. Okay and so um so

16:44 the pathogens coming in here is the reform of I. G.

16:49 And buying out these pathogens. Okay like I said this is early on

16:55 are formed typically in uh infection and finding isn't as as tight as you

17:05 but because they can give the conflict that's that's a benefit. Okay.

17:12 like I said we're not gonna go all the complexities of the human response

17:17 it can get quite complicated but uh is a fascinating subject. Um uh

17:26 you offer immunology course if that's something going to get all the dirty details

17:32 the process. But one of the is with T cells and B.

17:38 who I mentioned there's memory B cells there's also actually memory T cells as

17:42 and there's also learning curves. So is pretty expeditionary. Get better than

17:49 they do. Okay and so there's know like I said it's it's more

17:54 than than what I'm giving you trying give you more of the um you

17:59 basics of what goes on. Um Now it's not like I said

18:06 . G. M. Typically are first ones to respond that is robust

18:10 say. And then later on they overtaken by the I. G.

18:15 which represents more interesting for antibody Okay and uh much more accurate.

18:25 uh so I. G. The last one there's also a type

18:29 sits on a cell. And so mast cell invasive fields can contain these

18:35 um this is a kind of involved the inflammatory response for these chemicals.

18:41 remembers one of those that works on vessels more permeable. Um So uh

18:48 they can also be a problem. million analogy. Alright so um in

18:57 they're supposed to have a hyper response allergens. This is often the these

19:02 . G. Michael's buying bee pollen some other types of allergens and really

19:08 these cells of properties chemicals you know photographer response, things like water you

19:15 and you know we always think associated bad allergies. Okay. Um No

19:23 those are the five classes. OK so again these chemicals as a result

19:31 any questions about that? Yes. one comes second? The first one

19:37 . G. M. And then . G. G. We'll talk

19:39 we get to the the response in of the vaccination or infection. We'll

19:45 those that difference there. So I'll it up again shortly. Um Okay

19:52 here we are responsible for the other cells of what they do. And

19:56 remember it's it's about response to extra pathogens. Okay. Not not infecting

20:02 . So there's two ways this happens bologna um A. B. Cell

20:10 . Well for his sandbox. So way is what we call the

20:17 Um Yes general the tent. Okay now T. Cell dependent pathway so

20:29 T. Cell is going to activate T. Cell. Okay so here's

20:33 extra set of engines um and binding a B cell through antibiotic.

20:40 This could be I G. I. G. M. Is

20:43 what I can do this. So we just saw it can be in

20:46 size like the five headed monster Right? But it also exists as

20:52 . And they can also be a like a. D. I.

20:57 . D. And it's on top a B cell. And so by

21:01 engine and that kind of uh um um because also they also they have

21:09 as well ingest them. Right? then present those to the body.

21:14 so E cells have MHC class two cells uh dendritic cells and macrophages are

21:23 MHC class to everything else has Okay so um so the engine will

21:32 sell they will show that energy into body. Right so both by the

21:38 of your everybody and ingestion. Okay Uh so certain T cells responded.

21:46 was called T. helper cells. two. Yeah their ceo bind to

21:52 recognize energy and then cause the release cytokines that act on the ECE.

22:00 and that's what activates it. So it differentiates too and by increasing plasma

22:07 and memory B cells. Okay um so again the activation is dependent on

22:14 T cell binding cuba. Okay and is the most common way the details

22:21 activated effect. Um We're like a independent activation And those terrible involved.

22:30 large polymer type molecule policy. Soccer . There's a reason for that I'll

22:40 . But most of your engines activate cells through this mechanism. Okay.

22:47 so look at uh further into this . In fact the activation and the

22:56 . That's what we call this. Conal selections. Alright. So um

23:03 the Antibody production. Right? So can there uh attended it's like 10

23:10 the 13th popular combinations advantage and binding can be produced. Okay, So

23:17 means you can like to respond to anything that's out there. Okay.

23:22 has been number. Alright. And your B cells are unique in that

23:27 know, all the cells in your . Except of course your sex

23:34 But scared. Huh? The music hear in the horror movie.

23:43 Um To the Mhm. Um B um Oh yeah. Okay. The

23:57 cells um all ourselves are genetically Right? All the same D.

24:02 . A. Right? Um Except course, you know, gambits.

24:07 but the resales have a segment in genome that can be combined. And

24:16 how it can form these various engine types, sites on antibodies. And

24:24 it's a again it can form these different types of combinations, potentially responding

24:31 all sorts of types of management that be encountered. Okay so these B

24:36 populations that you have, Okay, mentioned. And potentially respond to lots

24:43 different types of cancers. And so what cool or set of them responds

24:50 course will depend on the presence of engine detective it buying into it.

24:54 . There is a very basic example just shows like four four pools of

25:01 . Right? What we call one two C three C four C.

25:06 , so encounter with a uh Okay, our ingenues let's say.

25:13 then and then within the engine But here's our red dots are the

25:19 . Okay? And it's pool number seed. I respond to it.

25:23 it has the antibodies that combined to . Okay, So that's the one

25:29 matches. Okay. And so then that population will literally. Right,

25:36 that's the clone expansion. Okay. called cognitive antigen. This pool that

25:44 hands because it's and it's the one it responds to the responds to.

25:50 . And so these are not close and we're gonna just make carbon

25:55 Right? And these are all The same identical handed things with the

26:01 identical binding sites. Right. And from a pool of plasma cells that

26:09 Okay, But then a bank of B cells that you hold onto.

26:15 , So plasma cells have about a of about 60 days. Okay.

26:22 then they go like all right, unless you stimulate that population again.

26:30 then they can produce, you so for that that figure in But

26:36 ourselves, those remain for 30, years and they have a long

26:43 Okay, now the numbers of those course wayne as you get older.

26:50 . To make So that was a population during the cells to the,

26:55 know, you know, over the and begins to kind of grow down

26:58 maybe they don't respond like they used and every for example, but you

27:04 he doesn't hang around for a long . You want them to write that

27:08 retained the memory of whatever the engine that they for a response to.

27:15 . So, um but that's really think the comes in memory cells.

27:21 , they can last a long but they do wayne. You

27:25 it differs to pay him the engine , But but it can be a

27:30 booster only 10 years or so. right. So, um varies depending

27:36 the type of vaccine. But so you're producing two types here are

27:43 that are immediate producers of antibodies, cells and then those that don't produce

27:49 . But hold on to that memory the engine they responded to.

27:55 And so the key independent activation. ? Not requiring a T cell to

28:03 cell. Again, it has to with these large types of antigens like

28:09 like this. Okay. And in the strongest and again, so when

28:17 say strong antigen, that means a a new response that's really strong.

28:24 get lots of anybody production tight by antibiotics. The types should have chemically

28:31 engines that are typically the best of . There's a large variety of

28:38 The infrastructure can be varied and second all kinds different properties for proteins.

28:44 so that tends to produce a stronger . Then you have to technically you

28:52 to have protein carbohydrates, fats, . Generally carbohydrates are okay. They

29:00 military a stronger immune responses proteins. proteins, carbohydrates, fats and in

29:08 war and fast um not a strong . Okay, so um so back

29:17 the t independent antigens. So here a of course can be a very

29:22 molecule. Right, big palmer. so it can bind multiple of these

29:29 on the surface of the resell. , so what it turns out and

29:34 , I'm not gonna expect notice but may help to to you know,

29:40 sure it's kind of understand this. it's about clumping together really somebody's antibody

29:48 the cell surface that's what you're called a B cell receptive. Okay,

29:54 just threw in this this figure here you don't you honestly, I'm not

29:59 test you on this but it helps know. Okay, so because your

30:03 doesn't really go into it. But so here's the police cells giving it

30:07 basic and a couple of antibodies. , so this is going to come

30:11 performance called and that's actually what So to do that you're gonna kind

30:17 bring these together. Okay. So can do it because antibodies have multiple

30:24 sites. Buy an engine can occur such what you call happy. And

30:31 process kind of creates that piece of there then activates cell. Okay.

30:38 uh normally have a contribution of the . Helper cells. Right? So

30:44 the T the deep end process. ? Um But a large like we

30:54 you can bring about much easier you bring them back with the coming together

30:59 these antibodies to so that's kind of going on, Right? It's so

31:04 . It can really bring together by its own right and create this beast

31:10 sell through this B. Cell receptor um and so it doesn't require the

31:17 of the T. Cell to help . Right? Because the engine's sell

31:21 and that's typically things like right so . But again the more common the

31:29 of the team Deep in what you about the T. seven process.

31:34 , that is more common in Canada's and aren't so big like this.

31:41 . Um very fortunate. Okay. . All right. So um so

31:49 , don't don't I just do this there for information first. Hopefully help

31:56 that's um Okay, so therapy Okay go ahead go ahead. And

32:06 I took that out uh and see you got the correct answer. Okay

32:13 uh so I'll talk about this while picking the correct answer. Okay um

32:20 . Secondary antibody response. So this to do with exposure. Right?

32:24 first exposure to either through infection, one way force or through vaccine.

32:36 uh this is a typical response. so um you'll get a longer longer

32:45 . So remember it's all about um detection, recognition binding. Right?

32:53 you get the output. That's going take some time as you see

32:58 Which I and then you note that the period here when you get through

33:05 the coast is more less time. left time upon second to go through

33:11 time. Right? That has to with the contribution of Yeah these

33:20 Okay. Oh that for details. . Very creative. We formed it

33:30 . Right? You for and memory , right? And then then if

33:37 get second exposure you worry about your cells are there ready to go?

33:41 so the second exposure will we'll activate . Uh They get time pretty much

33:47 because they're already they're already longer And so you produce um anybody much

33:53 in second response. So um the look at um the uh. Alright

34:05 next slide. Okay And go here sense. Okay so let's go here

34:17 this one. Alright so primary antibody . So we're gonna have again ever

34:21 be vaccination or through first exposure via . Okay and so uh the presence

34:32 antibody takes a little bit of And so with first form our GM

34:41 function. And uh but they're not and tight binding antibodies from this kind

34:50 when we were learning from here. ? So exposure to repeated exposure to

34:55 engine will kind of say strengthen the . Right? And you see that

35:00 the production of I. G. what actually happens in in in the

35:05 the that are responding to this and form plasma B cells and no form

35:12 . G. M. Okay, same B cells will then switch performing

35:18 . G. Molecules right? That and more stronger by any more

35:26 More more active if you will. . And higher quantity. Okay.

35:32 so I remember the GSR kind of all around type you know, compliments

35:42 , utilization, multi multi function type . Right? So and and high

35:49 but. Okay. And so but both types in this primary response.

35:55 . And then you have exposure to either to the uh the affection or

36:03 a booster shot. Okay. You've this bank of memory cells over form

36:08 they respond again with the same G. Very high response G.

36:18 . Okay so um but it's those memory cells that you are relying

36:26 Right? That's what you want to up And to be able to use

36:30 money. Heat. Right. 2nd , what have you? Right.

36:36 you know, this is of course basis for vaccination or immunization business.

36:42 , um between crushes back. so as we not yet. But

36:50 talk about vaccines. So knowing this the production of vaccines and how and

36:57 they work is of course based on on this. Okay. And so

37:03 T cells Okay um this uh so the T cells they of course

37:12 antigen. Okay, but T cells with with cells. Okay, some

37:22 with your own by myself and just settled in yourself etcetera that may potentially

37:28 infected. Okay. Um as on left, right, so your psycho

37:34 T cells recognize, remember all of body cells are MHC clash one try

37:42 so that's how your T cells you know, worried about yourself that

37:48 effective. Okay. And so so that those infected sounds there could be

37:56 to the surface. Right? And uh and of course it's safe being

38:02 right from the material, viral material an infection that infected cell can take

38:10 of that find intelligent BC long hill bring it to the surface.

38:15 And that's what you see here. . And so it will do.

38:21 through things that seem electoral. so a sort of toxic T

38:28 Okay, well recognized the androgen through T cell receptor and have a co

38:36 . Okay, so this is the that recognizes the class the MHC

38:41 Okay so this one specific for MHC one. So it's basically two

38:46 One by then. Body or Excuse me. And one that binds

38:50 the MHC molecule. Okay um now T helper cells and there's a couple

38:59 types. One type interactive macrophages and cells. One type there are actually

39:04 cells in fact but they do so these a different color receptors. So

39:09 one recognizes a class two. Okay then of course recognition to the answer

39:18 . So um so that's how you the how how these cells.

39:27 Um so this is all part of media T cells um is one that

39:37 recognize the virus because so for Okay um and the show it's true

39:44 co receptor which recognizes this this class modern feeling. So the engine and

39:52 antigens. What? Okay and so of course what you wanna do is

39:58 rid of this as far as effective get it out of here. Okay

40:03 that's the sort of topic T cells have enzymes and toxins to to kill

40:10 cell anything also introduce a apoptosis or ? Is that program So that so

40:17 can induce that much. We obviously to get this um Alright so we

40:22 sell on the population. Right And what that's what they do um Now

40:30 help themselves. Okay. They as seen already before I worked with one

40:37 of work with macrophages and dendritic cells these antigen presenting cells. Okay and

40:43 again through a different receptor. Okay uh receptors And uh before 24 and

40:56 so T. Helper one cells and . Helper two cells and T.

41:00 one cells activate macrophages. T helper activity E cells. Right so remember

41:09 this recall rather that this receptor is by um HIV HIV virus in fact

41:21 helped ourselves simply with that electric And so HIV can of course uh

41:30 population of these T. Helper cells you can see what what they're involved

41:34 . You know those that their types actively B cells time to activate macrophages

41:40 dendritic cells. And so if you're getting those guys out then you're obviously

41:45 the energy your adaptive immune system that . Um But anyways so uh the

41:56 sell me to the media. Okay so look at vaccines and their

42:01 You you want to try to get all activated. Right? You want

42:07 cells to become active. And um antibodies you want to ask you also

42:13 T helper cells and classic T Okay. And that's why vaccines that

42:21 be as close as you can to real thing bacterial infection. That's what

42:28 you the biggest response. Okay um when we get to vaccines I'll point

42:36 out. But it's kind of goals want to stimulate all the cell types

42:41 the adaptive immune system to get the response and longest lasting response. Um

42:50 here's a question that relates to this book surprisingly but just more terminology.

42:58 that complicated but kind of you can at the responses of your system.

43:05 categorized them, right? So that's to officially acquired active or passive.

43:11 so let's look at this first Okay. Which one is it we

43:19 talking about? Easy. Yeah. quicker question today. Holy cow.

43:25 all three d. Right there always free. So um so vaccination.

43:32 why does kind of seed fit? that's not the right. Um Is

43:42 right? Is that right? Is ? Let's see really. Um So

44:00 vaccination in the natural artistic clark? course. Obviously getting shot. Okay

44:07 not natural. Um And so the versus passive that's really Are you doing

44:14 work of making the antibodies or or ? Okay. And so the vaccination

44:20 course is artificially acquired and um but it's it's it's provides an basically to

44:29 use your body to make antibodies. it is an activist. Your body

44:33 actually doing it in response to to engines in the vaccine? Okay so

44:39 see is correct. And then down this one is about uh babies admission

44:47 and advised by the base. Okay um the uh um passive process because

44:58 get it through are getting preformed and making anything preformed antibodies but it's getting

45:06 ? Natural. Okay I'm not being with them. Okay and so you

45:11 have as well um you can have have the cupcakes. So uh infection

45:23 of course will be active, actively naturally required active meeting because of course

45:29 get an infection then you produce Okay um artificially acquired, passive you

45:36 you can go to the doctor was . It's not accommodated sharp I.

45:41 . Right uh uh as as a . Okay but of course you're being

45:49 these antibodies you're not making. So a passive process. Okay so um

45:55 unappreciated, acquired. Right so uh questions. Okay so it covered um

46:06 the immune system. So remember the between innate and adaptive. Right?

46:14 ? Dendritic cells uh coming together with as well. So um so let's

46:24 at a little bit about vaccines and . Okay so the uh so we're

46:34 about right this little vaccination. The exposure of the engine and then secondary

46:40 . And you get a bigger response I already have a bank of memory

46:44 ready to respond. And then um so this right here so this are

46:53 you might have seen this or heard this in the context of True.

47:03 and um so the table of the that are old that they're thinking that

47:09 a has a reputation number of representative how contagious a infectious agent. What's

47:20 ? So hi r. O number to a infectious agent that is more

47:27 spread of more contagious. Alright, that's 12-18 value. You see from

47:33 needs 12-18. Other people can be by Singapore slings or infected with and

47:40 Rather quickly into a number of Okay. So these will be more

47:45 than monks. Right. Are Okay. So then that our value

47:54 to an estimate of what you what would need to get to the population

47:59 fully vaccinated people for that Infection Okay. Measles. You need someone

48:06 range of 23-94% of the population fully . Thanks. So there are many

48:13 we will talk about it again on but it's hurting me and it's about

48:20 the majority of the population fully vaccinated they act as sinks to absorb the

48:29 people. Okay? So if um I'm here. It is. If

48:40 sitting here. Okay, that's Okay. And I have and I'm

48:46 vaccinated. But the triangles are vaccinated and most of the population is vaccinated

48:55 we have let's say there's another on vaccinated person here. Okay. So

49:03 me and me. All right, I'm a vaccine and this person is

49:07 . Okay. I've got a lot vaccinated people around both of us.

49:14 . So they act as sinks to the effective agent, which means likelihood

49:19 me getting it from somebody else's And we have all these accidents people

49:26 . Right so there's a certain You want to be at you're gonna

49:30 lots of triangles and vaccinated people. . Wanted her effect to take to

49:36 meaningful. Okay So um I feel the lower marks for the seminar you

49:44 need to have a minimum of 75% . About three quarters fully vaccinated because

49:49 everyone can be vaccinated one. They don't believe in it. But to

49:54 just can't mean dramatic reasons they can't . Um Or other things. There's

49:59 gonna be a proportion that can't be . So you try to do it

50:05 forties. Um very contagious and deadly . Pertussis, rubella particularly dangerous for

50:12 . Okay so um you of course to protect those that can't get

50:18 It only works if you get to threshold value right? Um are over

50:25 is on the low end. Okay is around the last I saw him

50:31 four 45. Um but that's still threshold of 75%. Are we in

50:39 U. S. L. And then reached that threshold fully

50:49 Look at it today I looked at a long time. I wouldn't have

50:56 . We in the US are So we fully vaccinated. Um The

51:07 of course there's differences across the country which stated the highest vaccination but as

51:20 I think California up there for sure new york, I saw the 77%

51:25 is 54% texas was 61% Alaska. don't know what they are. Not

51:35 . But but yeah, so it's And I think the last time I

51:40 right about six months ago we were like 58 or 55% I think.

51:46 we got like we had a surge the very beginning when vaccines came

51:50 That was like very swell. So were so but thankfully going down.

52:01 um anyway, so let's um look so I don't really memorize these

52:12 Okay, so again, it's kind more uh the this kind of survey

52:18 here is where the vaccines are Um which ones may be more effective

52:23 others. Okay. What forms will more effective than others? So you

52:27 have, we talked way back in beginning about attenuation. Right? Can

52:34 live vaccines, compassion, europe and . And so you will get my

52:40 your vaccines. This part of it the closest you'll get to the actual

52:45 agents. Okay, uh you whole killed organisms. Toxoid. Remember

52:52 toxins like botulism tetanus, right? know those those manages to use toxic

53:01 or what worked against toxins. so the tetanus shot is actually a

53:09 subunit. So now we get into realm of recorded DNA technology and following

53:17 jeans to produce just parts the interesting of the organs. Okay, Bradley

53:28 certainly my safety uh called virus black . You can mention that. And

53:35 uh so it's a voluntary backseat. this is gonna be the closest you'll

53:39 to the actual infectious agents. Um gives the best response because it is

53:47 to the real thing, right? activated through chemicals temperature but it's still

53:56 to replicate and that's the key. . Doesn't cause disease but it can

54:01 . And so it can replicate the . It can uh continue.

54:11 The other thing is um it will both hue, mural and sailor

54:20 Okay, so you can get into body cells, right? And that

54:26 turn into a set of toxic T can respond. Right? And then

54:30 of course and cells can show those E cell. So you gotta get

54:37 out there all these guys. And you can give a a really good

54:43 response. Okay. And so uh me see, just back up a

54:50 . So live attenuated vaccines. And see the long list here, right

54:54 with a long list of them right , measles, mumps, etcetera,

55:02 etcetera etcetera. Okay, so a of vaccines in that category. Now

55:10 inactivated killed. So these don't Okay, so it'll be in the

55:18 . Um and for green and they details can respond and produce antibodies uh

55:25 this really doesn't really uh affect. the T cells are not really so

55:35 response responders toxic. So um but safe right. There's a chance that

55:45 by the vaccine might revert right committee form. Okay. Not common.

55:52 making sure how how anyone is fairly event. But nonetheless a chance uh

56:01 actually really killed vaccines. But you you lose out somewhat on the how

56:09 the immune response robustness of it compared a vaccine. Um The sub unit

56:17 so different from the previous two whole organisms, bacteria. Well Um 70

56:29 are using parts of the antigens are of the organism, the angiogenic

56:37 right? The parts that stimulate the system. And this can be several

56:41 of this to just to purify protein . Um back in injected.

56:50 To um recommended vaccines. So you the genes when you chrome that floor

57:02 there. And then a lot of is really about the delivery system.

57:08 are you going to getting into the and you know, are you gonna

57:12 it get into cells and have them it? So the delivery is a

57:16 part of this. Okay. And among the common vaccines, So DNA

57:23 are vaccines, you know, better is acid vaccines, vaccines, vaccines

57:30 vaccines. Uh The other one is Conrad vector vaccine, J and J

57:37 . Um So again, you're manipulating genetic material um so that the the

57:45 will produce the get inside yourself and you transcribe and translate that region to

57:52 the energy in fact. Um So uh and that's the the virus virus

58:02 partners. Okay. So these are be made from viral proteins average self

58:11 to it viral unit. Okay. it doesn't contain the viral Gm.

58:16 it's not really the infectious unit. this great kind of box office

58:24 And you put your own engineer genetic in it to express the um

58:33 Um So uh different ways of doing . So again, always have a

58:39 part to either just type of the protein itself. Alright. Or would

58:47 like to hear like coach for the right. And none of these are

58:53 using the whole effective agents in fact parts of it. And so um

59:02 with these types. Okay. Um policy correct type. Because these are

59:09 used because one of the targets are capsules. The capital had created in

59:18 response being quite sacharow did not as necessarily be as protein type of

59:24 But remember the cholangitis organism you got for is of the type like this

59:32 the vaccine um the there are other of manufacturing to take acid basically just

59:39 . So we'll talk a little about . And so here's the vaccine.

59:45 , so again this article I sacrificed do the team um independent activation.

59:53 . But again it's not uh a response. Okay. You can enhance

59:58 response. Okay. Actually added a to the mixture. What are the

60:08 acronyms called? Conjugated vaccine facility? the it's a two part vaccine a

60:14 . So it has to play Sacha in there at the edge of then

60:18 a protein to it. Okay. that actually does use a stronger

60:23 Okay. You got involved in the cell now as well. Okay.

60:29 so he's to be stronger tech antibodies these types. It's just okay.

60:38 and so the fake acid vaccines. these are like what the code

60:44 of course the Moderna Pfizer is a vaccine. Okay, so here you're

60:52 the gene or genes and the engine it into a vector. Just fascinated

61:00 they can change that that portion. . And then you you wrote grow

61:06 plasmids up, right. Make a of thousands of copies of it.

61:10 then that's what becomes your vaccine. , here using this this term

61:16 Okay. Um and so basically just vessel to deliver. And so the

61:21 is delivered into the intra muscular Okay, so muscle cells are multi

61:28 eight. Okay, so that actually in. They begin to express the

61:35 . The system recognizes response to Okay. And so you get a

61:41 from both sides of the adaptive immune . Okay, so both B cells

61:45 T cells respond. Ah the the long lasting it is is the question

61:53 these these plasmids, I don't know long with their lifetime is in the

61:59 . And how long did your self keep keep producing? But um we

62:06 out that that's you know that the has a can wane after Sharon

62:16 Okay um because again these plasmids aren't . Alright so um we're coming effective

62:26 , this is like the J. . Vaccine is very common. Um

62:33 wait wait vaccine. So using a virus and event a virus which is

62:37 DNA virus has been used for this a long time. Mr Fergus.

62:42 so if you do is take advantage the ability of the virus to infect

62:46 cell. You take out the parts make it infections. Okay. And

62:51 replace it with a genome that will the genes of interest that okay.

62:59 you want. And so here you flu virus gene for this particular protein

63:07 the surface is H. A. and you insert that gene into this

63:13 that you've engineered and your delivery system this virus. And so the virus

63:20 contained the genetic information to produce that affect yourself then that angie was produced

63:27 then the immune system can respond to . Okay. Um so here's the

63:35 program vaccines. Okay so uh cheap you know about this by now I'm

63:43 you're seeing person these pictures a But the so the interest here are

63:48 spike proteins. Right? And that the information that makes those is what's

63:55 in the vaccine. Okay, so targets there and then two forms the

64:03 and then the. Okay so there the essential information and translate that to

64:14 the in this case the spike Okay. That um uh M.

64:22 then is is what is injected. . Uh next fight will show you

64:29 not just naked M. R. . That's being injected. That would

64:34 think it would be unstable and wouldn't that long. So it's delivered in

64:39 in a uh probably I think it's that he's making protected. Made plans

64:49 go. Okay. So um so so this kind of very simplified of

64:55 . Um are they going into the cell cell expresses it? Here's the

65:01 spike on the surface and now maybe just a response. Okay. And

65:07 funeral and some immediate response occurs. are neutralizing antibodies produce. Right took

65:14 virus virus came back um now the again. So here's our there's our

65:28 and RNA. So we're going to get all the eukaryotic elements to

65:35 Alright, it's gonna be translated. your tail. Right when we're talking

65:40 this in the three compared new materials throwing aerials and their genomes um that

65:48 a lot of processing that goes on you have to add things to the

65:52 to make it translatable. So that's all the elements are about.

65:55 so this and then here is the which is enclosed like this lipid

66:03 So kind of not a lipid violators you know it's meant to house the

66:08 . R. N. A. . And keep them up. Uh

66:12 bible and stable delivery system that once they'll uh entered the cell. And

66:20 of course express express the engine that they don't want the surface of the

66:26 , the game quarterbacks. Okay, vector vaccine. So again here it's

66:33 the genetic material that closure that spike putting into a viral genome.

66:41 And then putting it into the Right again this event a virus which

66:46 very well understood um has been magnificent not be infectious. And so especially

66:53 vehicle that will affect cells uh can to affect cells producing a good

67:02 Okay. Um so the uh again honestly this is not an R.

67:11 . A. Being injected but globally strategy but the same end result is

67:15 produce the spike protein that's obviously really commonly using that same but in different

67:22 . Okay. Um now the. . Uh Yeah. Yeah. If

67:35 not getting the article virus inside you why don't people feel sick when they

67:38 the vaccines? That could be a of reasons. So sickness from the

67:46 could be from often from things that that are part of the, oh

67:53 tried to purify the because the agent the process for delivery to somebody.

68:02 , there are gonna be certain types chemicals in there as like to preserve

68:07 maintain stability as those extraneous types of , not the actual engine that maybe

68:15 are reacting to. You can react these other kinds of chemicals that are

68:18 there. You will be purified and . That's where these things can

68:23 That used to be in the older uh used um when they cultivated

68:28 you often cultivate viruses and chicken embryos they would then harvest the antibodies to

68:35 the vaccine and it will often be parts of the chicken a reactions in

68:42 because oftentimes these byproducts that are part the the process of making the maximum

68:48 people react to. Yes, Okay, so this is again,

68:58 . So yeah, again, don't memorize this table. But you should

69:03 been, should I say in the versus the vaccine, you know,

69:08 make a difference. Is there? in the differentiation between the two covid

69:13 ? So these kind of things um have questions let me know. But

69:19 just more of a survey than anything . Okay, alright folks, see

69:24 on thursday.

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