© Distribution of this video is restricted by its owner
Transcript ×
Auto highlight
Font-size
00:21 Ok folks, let's get started Um 14 we only have a couple

00:33 five plants from that. So then . So 1617 immune system.

00:43 I'm gonna start the immune system a minutes. So that will go on

00:50 next week and then on to So back to weekly quizzes um

01:00 Uh So just be aware of that up due on monday. So uh

01:07 . O. Exam two was opened yesterday so I forgot to mention that

01:11 today's email. So uh do take look at it. You got

01:15 Uh let me know but give yourself chance to go through it, see

01:19 you can go through the questions. may just see if you can figure

01:22 out. If not I'll certainly let uh let me know. Okay.

01:28 Let's see. So our exam is for another three weeks yet but the

01:36 er for that will open next friday that exam. Okay so um

01:44 rapidly approaching the end here. Okay Let's look at so again as I

01:57 several times already, 14 is a of terms. Right? So you've

02:01 a a list here. I just literally just went to the slides and

02:08 just put them and group them all . Okay? So uh so this

02:13 really just writing these things out and remembering them. Okay. Um So

02:23 last time. Okay we talked about last very last thing we talked about

02:29 epidemiology. Right? So that's using data basically looking at data which are

02:41 regarding instance incidences of disease. and looking at it in different ways

02:48 it to, to um, maybe cause of the disease to find out

02:54 you can prevent disease. Um, to use it to, to figure

03:01 what's the source of the illness. there a particular demographic group that's more

03:07 to it? So lots of different to use the data? Um,

03:11 these are some examples here. There's ways. So what they described as

03:16 , analytical and um, uh, other one, the other one is

03:26 experimental. Okay. And grant there some overlap between these because they're all

03:30 at data. Okay. All three course are, but in um descriptive

03:36 I just realized Jon snow, you know who Jon snow is.

03:42 of Thrones. It's so that's not Jon snow obviously, although they're both

03:47 . I guess so. But mm The so he used, his

03:56 was kind of after the fact more less so color outbreak in London,

04:02 is very common thing during these times mid 1800s. I think people use

04:07 main river going through London that's kind their water source for everything both to

04:12 and dump into. Um, and water would be pumped there in various

04:17 with like a old fashioned, you not be aware of, you

04:21 back back in these days and you the water with one of these things

04:24 out of a spout in the middle the neighborhood. And that's where people

04:27 to collect water. And so just going around to these neighborhoods, he

04:32 basically looked at um death records of , People dying from cholera. And

04:38 um kind of went from house to asking okay, who who in your

04:43 had it, where were they at they became sick, these kind of

04:48 . And then kind of pieced together map of the area um in downtown

04:53 and saw a high number of cases the red arrow was at. That

04:57 traced to a particular pump and it a faulty uh contaminated or something when

05:05 changed it out to a brand new . The instances of cases went way

05:11 . But you wouldn't have known that you hadn't done this kind of these

05:15 . And so um that's what we descriptive. And so the analytical is

05:22 looking at a ton of statistical this is what Florence nightingale did.

05:28 looking at typhus, typhus is a that is really um a disease of

05:38 sanitary conditions, bad hygiene, close being together, um could be um

05:48 know, it's carried by fleas, types of fleas and ticks lice

05:54 many are carried by rodents, mice rats and things. And so um

05:59 just kind of like a fever and headache and symptoms become worse after

06:06 But it was a common in this and before this time it was very

06:11 because of course didn't have the sanitary we do nowadays in most places.

06:16 so that contributed heavily to that But she was interested in looking

06:20 you know, what is the nature this compared to our military,

06:24 Looking at military members of the military to just the average, you

06:29 civilians. Okay. And what is difference in terms of these cases of

06:34 ? And so let me flip flip real quick just to show you.

06:38 , he's just looking at this is looking at both typhus and cholera,

06:44 label that contagious diseases. She was looking at both of these, but

06:48 typhus cholera was a waterborne, you , people contaminated water. And so

06:54 course in the military, there were together at this time. You

07:00 they may not have had the best , uh, maybe not bathing

07:05 stuff like that. Um she especially for those that are just soldiers

07:11 were in England right, had a incidence and the general public.

07:16 .2 verse 18. But then we at soldiers actually in war war time

07:22 a I forget the Crimean war uh it was much higher. And so

07:28 attributed to that she attributes, she she investigated this and saw,

07:33 what's different here in this group compared these other two groups is the poor

07:39 , Right? So that's that's what immune system plus unsanitary conditions, poor

07:46 , poor um just day to day overall. And so altogether contributing to

07:52 uh these higher instances of typhus. so when she saw this and

07:57 well let's do X, Y and . To minimize these things get better

08:02 , cleanup, bathe regularly, etcetera. And of course instances go

08:09 down to 42 to 2%. Pretty . Okay. And so apparently she

08:14 had like 1000 page report with a of tons of graphs and data and

08:19 and things. That's of course that fits it. Being an analytical um

08:26 um epidemiology. Okay, experimental. kind of like uh basically taking up

08:34 experiment and a control group and in experimental group in similar ways. I

08:39 have briefly talked about this earlier, way back in the first chapter,

08:45 he instituted the use of uh antiseptics acceptance. And so in the hospital

08:53 was working at um he saw that in the hospital, the ward where

09:02 went to to give birth, that was a super high incidence of this

09:07 called childhood fever is kind of the term. Purple fever is the medical

09:13 is due to streptococcus bacterium acquired during . The baby uh can contract it

09:22 well as it can spread into the and then also affect the mother.

09:26 both mother and baby can be Um and so he said well what

09:32 what's contributing because he saw this group in the hospital that had a really

09:37 incidence of this disease and then he um you know women that didn't come

09:43 the hospital gave birth outside the hospital uh used the midwife that they outside

09:50 hospital that they were much lower instance this. And so he looked and

09:54 what's the common denominator here? Well these other groups um wash their

10:01 It was a regular practice of washing as a woman about to give

10:06 And in the hospital, the area maternity ward number women were giving

10:14 The doctors that did that were the doctors. So they would be like

10:20 2nd year medical students that would come of a uh cadaver awards. So

10:28 course as a doctor, you work cadavers to study the body and how

10:31 works and what not, they would directly from there to the maternity

10:36 Of course dirty and bloody and hands not clean and not privately. That's

10:41 what contributed to the high incidence of child bed fever. And so when

10:45 instituted said you aren't going in there you wash your hands. And so

10:50 that, I mean the numbers dramatically , much like the what we saw

10:55 uh with uh typhus, like a that's that like that very significant drop

11:02 again just washing your hands, So, um, but actually back

11:07 the day, it was a much soap to with this lye soap,

11:12 is actually very, almost like washing with bleach almost. Right? So

11:16 definitely gonna kill any bacteria likely kill of your own cells on there,

11:21 will definitely lead to this drop in number of diseases of this particular one

11:28 , referring to child bed fever. , you know, we all heard

11:33 clinical trials when the drug is on market then you test different groups,

11:38 ? Could be one gets a placebo doesn't these kind of things that all

11:43 into the the umbrella of experimental Okay, so, um, the

11:54 reporting. So I mentioned this already well. So case reporting and nationally

11:59 diseases kind of goes hand in Okay. So there are just quickly

12:05 do not memorize this table obviously. these are the nasty notifiable diseases.

12:13 what you might think, communicable obviously things like measles, mumps,

12:18 , um, uh, influenza Um, and then certainly all of

12:25 sexually transmitted diseases following this group, , and then certainly a number of

12:29 . Okay. And it's with this , of course, how you can

12:36 , see if there's an outbreak is what's going on and try to

12:40 that chain of transmission. We call . Okay, to to um,

12:44 contain the disease. So essential information have. So we can uh,

12:50 it's basically all that information is put together in this publication here.

12:58 . Which covers every infectious disease, think even non infectious diseases too.

13:05 on a weekly basis, you they track all this data if they

13:08 something that's, you know, spiking or what have you and report on

13:12 course and follow it to see it something significant. Um, you

13:18 if you're interested, you know, just google that and you can see

13:21 actual weekly reports here. But once the end of the year are kind

13:25 interesting. It's kind of a review the previous year and the it has

13:31 infectious disease and the number of cases during the year. Um, but

13:37 so with that the terms you see and mortality. Okay, So,

13:45 , I'm sure you've all heard of , obviously mortality rate. The number

13:48 deaths. Right. It's about deaths these diseases, morbidity is the symptoms

13:55 rather the instance of a specific Okay, you don't necessarily die of

14:00 . But you reported two people reported have it. It's been confirmed from

14:06 that they have the disease. whether they fall into the mortality

14:11 of course, depends if they die number than mortality, Mortality and morbidity

14:33 . That's like 100% mortality rate. get the symptoms of disease and you

14:37 . All right. So you're not to be the same. Okay.

14:42 mean, I guess it be close it was something like Ebola, but

14:46 with that it's not equal. So morbidity is gonna be higher.

14:51 You have a lot of people that down with influenza, right, contributing

14:55 the morbidity numbers. But how many gonna actually die? Much less?

15:00 gonna die than actually? Yeah. that make sense? That morbid is

15:04 to be immortality how they relate? . Um Okay, so I see

15:13 that ends 14. Okay. Any about it? Okay, so let's

15:21 so we're going to in a So two parts here innate and adaptive

15:26 immunity 17. And that 17 is of those uh you're gonna kind of

15:32 on it yourself? Right. So I think the material should be

15:38 the lecture video and stuff. So ahead and take a look at that

15:41 already. For 17. For Okay. And we'll go through that

15:45 Thursday. Okay, I'll have a of questions and kind of frame it

15:51 that. So you've seen this already times, but again, just to

15:56 we're not gonna focus on this is this really host offenses. Okay,

16:05 which of course relates to, you , do you come down with

16:08 What's your level of resistance or you're so resistant? You're more susceptible.

16:14 . Of course, that relates to your immune system obviously. Okay,

16:19 with the innate immune system, that's you come out of the, you

16:24 , come out right, you're born boom, you've got that innate immune

16:28 already working not, you know, a baby, obviously not at the

16:32 level as it will a few months years from that point, but you

16:37 have obviously skin, that's a physical , certainly part of the immune

16:41 You have mucous membranes lining your body and whatnot, That's that's part of

16:46 . Um We call the innate immune non specific. Okay, and there's

16:53 reason for that. But let's look at this question here, just to

16:57 if we can come up with something . So remember, so as we

17:01 through this, your your innate and immune system, you can look at

17:06 as 12 and three in terms of . And one way to visualize that

17:12 really if you're a if you're a out here, right, and it

17:17 to the body. Okay, what the layers it's going through?

17:22 As it penetrates deeper into your if it does. Okay, and

17:26 that's one way to look at it terms of first line, second

17:28 third line. Okay, um let's here. Um so as you're answering

17:39 , so specific versus non specific. specific the immune system is the adaptive

17:46 system. Okay, because it relies on binding of components to each other

17:57 antibody very often. So there's there's definite specificity to it because it involves

18:02 binding to an antigen. Okay and what sets in motion. All the

18:08 that follow. Okay your innate immune is not oh there is molecules binding

18:15 certain in part of the process. not all centered on that, it's

18:21 microbes coming in and you have different that they can encounter and may or

18:27 not get through but it's not as as adaptive system. Okay So let's

18:33 down here from 10. Alright. Yeah that's uh yeah it's corrected fever

18:51 is is I think more of a line of defense. Okay and so

18:57 look at um both sides of this here. Here we go. So

19:04 not specific and specific. Okay so new system falls into that category.

19:09 specific. Um So first line so I said picture microbe here is coming

19:15 what's gonna encounter first skin skin barrier if it gets into your nose or

19:21 maybe mucous membranes line your nasal Um You ingest it right? Your

19:28 membranes coat your throat and then your . And so basically a colleague of

19:35 that teaches A. And P. human fit said this gives the analogy

19:40 the body is a donut. Okay right through right? So your mouth

19:46 alright the whole right exposed to the right? But they have your fist

19:52 your guts and everything else around So of course uh what goes through

19:56 hole is what you breathe in And of course that will contain uh

20:03 with everything encounter right in the mucous as they pass through. So um

20:10 skin membranes and don't ever forget your own microbiome right there. They're part

20:17 that certainly as well. Okay now going to be somewhat redundant because um

20:25 your first line defense you can look these especially um skin and mucous membranes

20:35 as a physical barrier. Okay. they also produce a chemical barrier which

20:42 skin and mucous membranes produce chemicals and chemicals also can interact and uh counteract

20:52 that committee. So so your first of defense is both a chemical physical

20:57 chemical barriers as as you'll see um line defense. So getting past your

21:05 line then. Second line I kind characterize as cells specific cells that are

21:12 to interact with pathogens to get rid them and also processes. So I

21:17 like inflammation fever. These I call these of course are particular cell types

21:27 now. Even the processes of course cells. Okay but you when your

21:32 ways to fight infection of course is figural psychosis, literally just engulfing pathogens

21:39 breaking them up license. Okay so a number of number of cells and

21:46 processes that are part of the second of defense. And so the third

21:49 which will will get to until next from the day is your data review

21:55 . So this requires um it only activated. Okay so they respond two

22:09 what activates that system. Right? And so uh that's why we have

22:17 that's what we call it specific. you have cells in your immune system

22:22 the immune system we'll recognize antigens. um antibodies is one way production of

22:31 . You can of the thousands if millions of potential engines out there.

22:36 can likely produce antibodies to each and one of them allergies are about kind

22:47 a hyper response to certain antigens and any case the uh and so T

23:09 and B. Cells and also a other types. And we're also going

23:18 see is that there will be cell that will bridge that both sides you

23:29 cell types that both are part of adaptive and DNA. And so they

23:34 kind of connected to. So um knowing I just told you now let's

23:43 see this is a this is a response faster right. Or the

23:56 So I'm gonna have to run the on this one. Hey winding

24:29 Alright count down from four. So it's definitely gonna be an eight and

24:40 really has to do with that that to Well the energon the energy in

24:49 or response to energy which is what adaptive immune system relies on.

24:57 Um There are 2 2 things. is um identify. Okay,

25:09 Find it so to speak. And then bind it. Uh It's

25:22 be very not scientific but I'll just new stuff. Okay, I'll elaborate

25:32 that. Of course it's a lot that. But do stuff means um

25:38 identifying to recognizing, finding it There's a time element that doesn't happen

25:43 , right? Uh then bind engine then that then induces a lot of

25:51 going on inside the cell. making different types of molecules etcetera

25:56 And then um that that then leads so they do stuff is then does

26:02 believe or sell itself buys an engine then stuff happens. Right, More

26:07 happens. So it's uh for now is this is why we'll get the

26:13 and bolts next week. But um yeah, this all takes time.

26:19 of course the native resources right Right. It's a better it stops

26:25 so again, put the kind of terms in this chapter together here.

26:34 we get I broke it down and of chemical defenses, physical barriers,

26:38 mucous membranes, right? Um Different types we see here. Okay.

26:47 Another cell type here that the immune relies on Auntie Gin. This is

26:53 one side to kind of something you'll over and over. Okay. So

26:58 it's basically a generic term chemicals that basically tell other cells of the immune

27:07 what to do. And they have variety of different functions as you'll

27:12 Um And names. Right? The kind of a generic name but their

27:17 names for all these things um and there are some processes here in this

27:24 . Okay. Um pam oops. . Not sure what that is

27:29 We'll talk about it. Figure The other thing is the type of

27:37 your body has to deal with. . Will require two different strategies.

27:46 you're gonna have pathogens who do their . So now this is in your

27:52 . Okay. Do their thing by outside yourselves. Right so we call

27:57 cellular pathogen. Okay. But then types that go inside yourselves and that's

28:03 motive infection viruses. So you have interest cellular and intracellular pathogens but you

28:11 to have two very different ways of with that. Okay because when a

28:16 is inside itself it's kind of hidden the body. Okay. And so

28:22 has to be a way to identify kind of infected cells and there

28:26 Alright so so they're gonna be way deal with both. Okay so you

28:32 the rule of thumb typically is fabulous . Won't work if it's inside of

28:38 cell. Right? Certainly if it's susceptible to fake a psychosis engulf it

28:44 chew it up. So we'll see are several strategies for what type of

28:50 is how we can be used to it maps. Okay champs champs

29:14 A. M. P. Yes it's so two operative right for

30:41 . Um And so and also your doesn't go into it and I'm not

30:46 touch you on it. Cells have . We have a bunch of cells

31:24 your body that have peace. Um And when they encounter passages like this

31:32 that that signal sort of a defect sets into motion the production of

31:41 Okay as I mentioned you have a of different functions. Okay. From

31:47 a few. Okay I will mention as we go through but uh come

32:31 With Octopus with a bunch of eight right? That would be an active

32:40 no arms. Right? That's an the part of me. They infection

33:04 is to get yourselves to that And so chemo taxes right? This

33:11 toward a chemical and so that's what does. Okay so if you have

33:16 skin cut or wound or something here whatever these chemo tactic signals will draw

33:24 immunity themselves there. Uh inflammatory response um That will go through that.

33:31 today. But next time. So these are typical responses. We've all

33:35 fever. We've all had inflammation. ? These are specific responses really.

33:41 is really about um containing that's just where it entered the body so to

33:51 . So we have like a splinter it's contaminated and you have an infection

33:56 the inflammatory response was meant to kind continue right there and not let it

34:02 . Um fever has its own use activate T. And B. Cells

34:09 that's activating the adaptive. So again are just four things five things but

34:15 of kind of doing a bunch of stuff as well. Okay all all

34:20 of activating some part of the immune . Okay so back to what so

34:26 of this system on this slide here total like receptor system right This is

34:33 like it's it's it's like pulling the smell smoke in the building and you

34:41 the fire alarm to alert everybody. kind of what this is kind of

34:47 alert the body let's get let's get kind of thing. Okay and I

34:54 do that and outside of kinds because will get certain cells to respond as

35:01 . Okay so to like receptors kind the alarm system so toll like receptors

35:07 these things. Right these things do kill anything. Okay they don't have

35:13 role in killing a pathogen. Their is in warning the body of a

35:19 pathogen is present. And let's get do something. Okay that's what it

35:24 . Right? Um so again it's obvious to you but the total receptor

35:32 not a cell is a protein on cell surface that interacts with a

35:38 A. M. P. And activates it. Um Okay so first

35:43 defenses so it's gonna be a little redundant as I said. So we

35:46 at it first as a physical So skin of course is a very

35:52 thick layer of multiple layers of Okay epithelial cells. And so that

35:59 itself provides a strong barrier. But you put in this kind of protein

36:06 that kind of holds it together and it keratin, keratin. Okay keratin

36:11 very and it's on the surface of body it's very thick on your fingernails

36:19 your fingernails are basically tearing your Okay. But but your body is

36:24 with this skin is covered with this well so it makes it very almost

36:29 Impenetrable but very stout barrier. But do have of course natural openings in

36:35 skin. Right? You have Right? Sweat glands, hair

36:41 So these are kind of can be openings where bacteria may be able to

36:45 . Okay and of course you have cut or otherwise away from bacteria to

36:52 your skin through a wound. That's what we call subcutaneous infection. So

36:57 membranes of course line which means that G. I tract obviously G.

37:03 track respiratory track etcetera. Okay and simply have a structure like this a

37:11 we often call a basement membrane. need to worry about that term.

37:16 as the blue kind of like the on top of that you have various

37:21 . This would be cells from your goblet cells are part of that.

37:26 And so but again very thick, and often producing uh always hold your

37:35 . Remember to produce some sort of secretion. What's the mucus is a

37:40 right to keep the cells moist uh the intestine and serves also the function

37:45 helping food pass through. But mucus nature of it can also help track

37:54 uh plus your your cilia in your form this thing called Salieri. You're

38:15 felt to see 54 3 uh and hair and track stuff right? Just

39:10 the cilia in your throat. Um and saliva. Uh So you always

39:18 your eyes. Well some are your but that you know, tears are

39:25 that to kind of keep washing wash microbes up, live what wash

39:31 your teeth and whatnot. Um So then as well earwax, earwax does

39:38 a function. I think that maybe trap bugs in your ears.

39:45 it's gonna be bugs as well, insects anyway. Um but certainly digestion

39:52 ? You eliminate lots of facts, past your system. Uh epiglottis,

39:58 the cover your wind pipe wall. you don't get things in your

40:02 So yeah all these are part of helping kind of prevent at least as

40:08 they can microbes from getting into your and where they're at more or

40:13 Okay so again all of these, of these will also act as chemical

40:20 . Okay so because they all have tends to be kind of a salty

40:29 acidic because the kind of molecules that produced there. And so that in

40:33 is a way to kind of um effect we can actually live there.

40:39 , staphylococcus like those conditions with july is one of the main bacteria you

40:45 on your skin. Another one uh . So survive a gastric juice.

40:52 very low ph um vaginal secretions. acidic urine is also actually slightly acidic

40:59 the one common thing in all many these is circled them here is

41:04 Okay in multiple places, write down right hand, is that material That

41:17 what they're so only. Okay so so definitely a defense against the bacterial

41:24 um that happened so long. And again as mentioned before we talked about

41:30 that this is part of your innate system as well, your microbiota.

41:35 their mere presence alone keeps other things taking hold um and they produce their

41:44 kind of micro environments that can oftentimes things from so very essential. Um

41:53 so first line uh physical and chemical then after them are second line.

42:01 so we start with kind of different types uh specific cell types involved.

42:06 you break down blood plasma fraction, centrifuge it um you have a protein

42:14 , the platform that contains anti biasing and other types of proteins. The

42:22 other part of this contains what are form elements. So red blood

42:25 Red blood cells um Our basically our sacks of hemoglobin and hemoglobin binds

42:37 Okay uh red blood cells don't have nucleus. Okay. Um But uh

42:45 also are not really cells are fragments involved in clotting but the cell types

42:51 course are your leukocyte, your white cells um of various types. And

42:56 these terminology of the granule sites and granule sites a little bit deceiving because

43:05 they all they all can have Okay, it's just that way,

43:12 at them under a light microscope, much more obvious in these types

43:18 Basic skills you look at and go that's a that's a grainy appearance.

43:22 . Not because they have lots of . Okay. Um It's just not

43:26 visible under a microscope. But these although although they do have but anyways

43:33 sometimes with terms it's a historical thing it never changes but that's that's how

43:38 still in front of the granule sites a granule sites. Um And so

43:44 go through each of these here alright neutrophils are gonna be your Early on

43:52 is neutrophils that are your primary fake cell types that do the bulk of

43:59 work initially. Right? Um so are in blood. So you see

44:05 70%, don't worry so much about percentages but just to show that they

44:12 in the highest quality of your And so if they're in your blood

44:18 you have an infectious agent that's in tissues outside the blood, right,

44:23 you have to get them out of blood into the surrounding tissues.

44:28 And that's what interferes do. so the exit blood is all part

44:33 that inflammatory response which was going next . But it's uh but you

44:42 aren't you floating around everywhere in your , there in your bloodstream? And

44:45 have to get them out of the . And there's a mechanism that they

44:49 let that happen. But they are primary infection fighters early on, they

44:52 taken over later. They um One thing. So you might look at

44:59 these cell types. They have like weird um morphology. Well they look

45:05 inside. You have these purple this is actually the D.

45:10 A. Chromosomes and they just form like sacks inside. They're all

45:17 But that's just how they look. what they call them, polity morpho

45:24 , probably more like it means many kind of nucleus just kind of a

45:29 future of those types. Basic So basic fields, unlike neutral fields

45:35 not specific cell types. They're thing to um release toxins typically and other

45:42 of cyber crimes. And so um so um lots of chemical services,

45:57 basically the amount in their blood is that high. So uh if you

46:02 hay fever, things like that, can probably blame your basic feels

46:06 Um so these are big acidic uh this big contributors and inter fields but

46:16 they do can act is in very pathogens by large. I mean we

46:21 about these worms before, right? those those can be attacked by

46:26 Their their thing is often to produce of tires and they actually interact with

46:33 pathogens. Um so again large practically like a big helmet or something like

46:41 right center field will be attracted to site and they actually interact with um

46:51 react with antibodies. So we'll see antibodies will interact with different of your

46:57 system selves in different ways. So antibodies our antibodies to the worm that

47:06 fills can also bind the antibody. then you get these all together.

47:10 a way to kind of collect a of sender films together so that when

47:15 release toxin right? You have a of toxin. So it's a way

47:20 concentrate center fields around the big right? Because you're gonna have to

47:26 have a lot of toxin and take of these things down. So you

47:30 get a bunch of center fields there have them hook onto the thing then

47:33 will release a toxin altogether and take down. So it's kind of how

47:38 work. Um so but again these these fully grown things are investing in

47:47 . B. Is short for Okay so like I said, you'll

47:55 see interactions between withdraw antibodies kind of this right? Like a why why

48:03 And these are all points that can . And so these this part

48:08 the two that are close together those and the bottom part is one that

48:13 buy into a cell type right? of some sort and even if it

48:19 one type that can do that, others that you'll you'll see as

48:22 Okay. Kind of jumping the gun but because I'll repeat this again but

48:26 we're here it seems like a good . Um So let's uh don't worry

48:34 you can get this thing wrong because gonna go through it again anyway when

48:38 get the antibodies and antigens. Um let's see what else is here we

48:45 . Okay so a grandiosity. These your macrophages. Dendritic cells. So

48:52 macrophages and dendritic cells start out as model site. So motorcycles circulating the

48:58 . But then they go to your system. Your lymphatic system plays a

49:05 part especially in your adaptive immune Okay so your B cells, your

49:11 cells macrophages. Dendritic cells they kind hang out in your lymphatic system,

49:16 what they do. Okay so if have had an infection and your doctor

49:22 this on your throat, right swelling maybe your armpit swell. Okay and

49:30 get painful. Um They're highly concentrated lymphatic vessels, right? And so

49:36 swell because the the cell types in are growing and proliferating right to fight

49:41 infection and that's what caused the Um The uh but they are so

49:48 macrophages and dendritic cells are specific but have this function. Okay, they

49:56 antigen presenting cells. So again these cell types that link up with the

50:01 immune system and uh and they can activated by your activity system. Have

50:11 functions there. Okay so engine presentation a big function that really has to

50:18 with um to alerting the body to their pathogens. I'll hold out for

50:28 . We'll wait. But energy building or a pc. They're also called

50:35 short text. So I'm adventurous Okay Now, very recently they are

51:26 of trying to exploit this activity and by genetically fixing natural killer cells to

51:35 able to be better at this function recognize different types of tumor cells.

51:41 using it to be a cancer fighting . Okay. There's a lot of

51:45 being done on that at the medical on that. Um But our context

51:50 we're looking at cells are infected. , so what happens is let me

51:58 I'm going to I just need to real quick to see. Okay.

52:02 it. Uh So the MHC that's the thing we need to talk about

52:08 affects a lot of different things Okay. So uh so natural killer

52:14 to look for infected or cancer So the thing is elaborate here in

52:19 second. So if your cells have certainly have different types of molecules on

52:28 surface. Okay. I'm just and of those and as opposed to your

52:36 healthy cells have all different types of on the surface, but they also

52:42 have and see energies. Okay, just drawing it like this just for

52:48 obvious. Um So the think of as a barcode there, you're a

52:59 on all of yourselves that identifies the to yourselves. So it's your own

53:03 barcode on all of yourselves comprising all tissues. Okay. So and they're

53:10 to be there. Okay, when not there, that's the signals,

53:15 . Weird. Something's not Right. . So if they're lacking or if

53:20 are only very few this or this they lack or have one or

53:28 that's something weird. The body that's not right. All right.

53:32 so that's what natural killer cells look for. Okay. And so they

53:36 of I guess they kind of hover the cells and they can recognize that

53:40 got the usual are supposed to have things and it's lacking. That's the

53:47 . Right? That cells not what supposed to be something wrong with

53:51 Okay I'll be infected. Okay. so infected cells like with a virus

53:58 other types, They can alter not of them, but many can alter

54:03 happens on the surface of the The types of things that end up

54:07 . And that's what natural killer for example, can detect that.

54:11 then the signals get rid of the , get it out of the

54:14 It's ineffective. Something's not right. also cancer cells can also produce that

54:21 appearance. Not all cancer types, some can and that also is a

54:26 of the cells not normal. Get of it. So that's what natural

54:29 cells do. Okay. Kind of for that. I'll elaborate. And

54:32 may see engine second, but that's of what any questions about that.

54:38 that's that's kind of what they Okay, so um so when they

54:43 bind, what do they do? , they I can hear it make

54:48 easier. Let's do this race. , so when they bind to

54:59 so they will um secrete these So preference. So think of

55:08 If you perforate something, you put punch a hole in it.

55:12 so preference is kind of like Almost protein tunnels. They stick into

55:16 cell and stuff we cut and the . Okay, enzymes are enzymes.

55:25 apoptosis is a feature um it's a feature of all yourselves. It's what's

55:33 a programmed cell death. So when cells are age and they don't work

55:39 anymore. Or something else damages The body says kill yourself, go

55:45 apoptosis basically. Right? You had sunburn, right? And you got

55:51 skin was peeling, That's the way see. It was red, it

55:55 hurt. And eventually the skin That is basically apoptosis going on.

57:44 the uh ability to come, what refers to is his. So oh

58:24 underneath. So you have two right? one and 2. The

59:06 way when I said uh huh. different. That's how uh with these

60:17 in different ways um and create different . Okay. And those effects can

60:24 the parts effect itself. Okay. it lacks MHC antigens, it'll be

60:29 rid of. Okay. Um the other types interact with other T cell

60:40 , interact with macrophages etc. We'll about that as we get into Chapter

60:45 next week. Okay. But the is, it makes the engines it's

60:49 critical to have a system like right? Otherwise, if you had

60:53 infectious agent in you, how would body know is even foreign or

60:59 Right. So you already have a in place with all your cells making

61:03 all your tissues that have those barcodes on them that are telling your body

61:09 is yours. Okay. So if else comes in that doesn't have that

61:14 then your body can say, oh something, not right, Foreign.

61:18 an agent, right, Do something it. So that's having that system

61:22 place allows you to detect something that's part of that system. Okay.

61:28 of course there's even times when your will attack its own, right?

61:35 your auto immune diseases. Right? certainly tissues become, you know,

61:40 body does fight them. That's you , for other different reasons. But

61:44 having a system in place like this you to detect something that's not not

61:49 same as what what that is. pathogens some sort. Okay. The

61:55 system as mentioned is an important So it's not um in terms of

62:02 immune immunity, the be checked against types of things you breathe in things

62:11 eat. Okay. Your your lymphatic will um can be particularly dense in

62:18 parts of your body. Like your particularly dense in lymphatic tissue, your

62:23 your throat, uh very dense. growing areas very dense tissue, swear

62:31 T cells, B cells, Dendritic cells hang out okay? Um

62:40 uh the uh and your spleen has synthetic tissue. You can filter out

62:47 in your blood for example. You have uh lymphatic tissue would concentrate

62:55 different parts of your skin, under skin, your intestinal wall.

63:00 And so how the lymphatic system uh it's a system of vessels of

63:06 But unlike vascular system, there's not heart pumping in fact typically move through

63:16 and through muscle contractions and through the of your arteries and arteries and

63:25 And so your arteries because lymphatic vessels very close to these things. Okay

63:29 so that kind of assists in pumping basically with lymphatic fluid lymphatic system is

63:37 for is to pick up fluid that's from your capillaries. Right? So

63:43 veins and arteries um intersect very very one cell thick vessels called capillaries.

63:52 called capillary bed. And um that's these are concentrating your vital organs.

63:58 so it feeds them, right? you exchange materials in the capillaries,

64:02 waste back and forth. And of when that happens you lose fluid from

64:10 blood volume, You lose fluid from vascular system. So you have to

64:13 able to recover that and dump it in. Right? That's what the

64:17 system does. It collects that what's interstitial fluid. Okay. It collects

64:23 and basically it dumps it back in here around your clavicle. And there's

64:28 where it dumps back into your cardiovascular and so it kind of helps to

64:33 blood volume and and because you do fluid from your cardiovascular system and that

64:40 pick it up. Okay. But it's a place where your these cell

64:46 reside. Okay. And so it's important for that. Um Now here's

64:54 example of your intestinal uh kind of lymphatic tissue very dense in your intestinal

65:02 intestines is in these pirate patches. , so very dense. And what

65:07 looks like in there is you have kinds of what are called m cells

65:12 between your normal kind of cells in intestine that are about absorbing food and

65:18 . Right? And so here are microbes coming through. You have um

65:24 system cells and macrophages and things that any kind of microbes that are that

65:30 in there to get rid of And so you'll have these is a

65:34 section and you see the dense tissue here pires throughout your intestines. Okay

65:44 so here so figure acidosis. Okay again this is one of your main

65:52 fight infection. Okay so your primary are macrophages, dendritic cells and um

66:01 . Okay and so in terms of they can be what are called wandering

66:08 fixed. Okay so wandering like the implies you can travel throughout your lymphatic

66:14 uh wandered around engulfing you know pathogens have you fixed or stay in one

66:22 . So very common to have for al Viola macrophages living a lifetime in

66:28 lungs and they pick up any kind microbes that might be there. Um

66:34 so the grandiose sites like neutrophils, , infections early in the infection

66:47 how this happens. So first get or dendritic cells to the site of

66:58 number one that's chemo taxes then stick the pathogens that part of that is

67:05 engulf mint process. Take it in then break it apart license. Okay

67:11 the four step process. And so so here you see here's a

67:18 Okay. And part of the binding is these pants, right? So

67:25 not just ingesting and figure sensitizing the but also releasing set of alert other

67:33 in the body. So they have as well. That and so um

67:40 is something we'll talk about later. the uh sometimes you have microbial types

67:49 are easier to buy it easier as be taken in than others. Other

67:55 are maybe have a very thick Okay. That makes them less able

67:59 be bound and taken in. That's it's a virulence factor. And so

68:03 do you deal with that? Will produce other chemicals that can code

68:07 And then that can be taken That's what do right. Something like

68:12 complement these coat the pathogen and then what's taken in. It makes it

68:19 to figure ties. Okay, the part. So you have a vehicle

68:27 it's engulfed right into a vehicle called figure zone. And then our feeding

68:34 . And then that fuses with the all Okay. And that's kind of

68:38 digestive organ. L that will then down the microbes either through production of

68:45 radicals. We talked about that Um these are toxic to the cell

68:51 have license line to break down cell and ultimately getting rid of it.

68:57 , now the thing about a about is these can also the particles that

69:07 you see some of these being These can also be the NHC module

69:15 these can present. And so microfiche also be an engine presenting cell,

69:20 ? A Pc. And they can that by taking some of this material

69:26 with MHC molecules in the cell then to the surface and now the engine

69:34 visible to the immune system. That respond in a different way.

69:41 that's what the engine presenting cell does you, allows the body to see

69:45 engine and respond to it. if I hadn't seen it before.

69:50 um the so I just mentioned about optimization, that not everything is easily

70:00 with thai so that's things like a capsule typically aren't. So they enhance

70:05 you can produce antibodies to it. then those antibodies are bound to the

70:12 . Right? And then the cell has a receptor that combined to that

70:18 the antibody Right? And then the thing gets taken in. Right?

70:24 it's a way to make something that not easily monetized. Okay, similarly

70:29 same process can occur. You can it with antibody compliment compliment kind of

70:37 soluble protein factors. So that can to sell and communication as well.

70:45 it's a way to figure these things aren't easily fixed. Okay,

70:50 observations of the molecule that code so can be an antibiotic compliment optimization is

70:56 process of taking it this way. . Um, that's a good way

71:03 pace. To stop. Right, . Thanks for hanging in there.

71:07 , we'll see you next weekend and

-
+