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The Innate Immune Response

The Innate Immune Response. FUNCTIONS OF THE IMMUNE SYSTEM: Recognize , destroy and clear a diversity of pathogens. Initiate tissue and wound healing processes . Recognize and clear damaged self components. Exhibit “tolerance” to innocuous material including self.

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The Innate Immune Response

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  1. The Innate Immune Response

  2. FUNCTIONS OF THE IMMUNE SYSTEM: • Recognize, destroy and clear a diversity of pathogens. • Initiate tissue and wound healing processes. • Recognize and clear damaged self components. • Exhibit “tolerance” to innocuous material including self

  3. The Normal Immune Response • The normal immune response is best understood in the context of defense against infectious pathogens, the classical definition of immunity. • Innate immunityrefers to defense mechanisms that have evolved to specifically recognize microbes and protect individuals against infections. • Adaptive immunityconsists of mechanisms that are stimulated and are capable of recognizing microbial and nonmicrobial substances.

  4. Innate immunity • The first line of defense always ready to prevent and eradicate infections. • Adaptive immunity • Develops later, after exposure to microbes, and is even more powerful than innate immunity in combating infections. • By convention, the term “immune response” refers to adaptive immunity.

  5. Innate and Adaptive immunity represent two different arms of the immune system that work together in host defense. • Innate Immunity (natural/native): • Provides immediate protection from infection. • Is broadly specific to microbes and tissue damage products. • Does not change in response to reinfection (nonadaptive) • Initiates processes that lead to activation of adaptive immune responses. • Adaptive Immunity (specific/acquired): • Appears to adapt to a variety of non-self components (acquired) • Is highly specific to a particular molecule “antigen” • Responses upon reinfection are faster, better and stronger (memory) • Generates proteins and cells that enhance innate immune function.

  6. http://classconnection.s3.amazonaws.com/536/flashcards/1317536/jpg/paneth_cell1332475911026.jpghttp://classconnection.s3.amazonaws.com/536/flashcards/1317536/jpg/paneth_cell1332475911026.jpg INNATE IMMUNITY A major components of innate immunity are epithelial barriers that block entry of microbes. Epithelia of the skin and gastrointestinal and respiratory tracts provide mechanical barriers to the entry of microbes from the external environment. Epithelial cells also produce anti-microbial molecules such as defensins, and lymphocytes located in the epithelia combat microbes at these sites. If microbes do breach epithelial boundaries, other defense mechanisms are called in.

  7. Skin http://www.bbcm.univ.trieste.it/~antimic/images/ampmech.jpg http://ars.els-cdn.com/content/image/1-s2.0-S0091674912035634-gr1.jpg http://4.bp.blogspot.com/-IlBLt5vn9Js/UKEWss4UTMI/AAAAAAAAByU/tSRUZjiBwxc/s1600/SKIN+LAYERS.jpg

  8. Lung http://cmr.asm.org/content/24/1/210/F1.large.jpg

  9. Gut Defensins are antimicrobial peptides http://www.nature.com/nri/journal/v9/n11/images/nri2655-f3.jpg

  10. The two most important cellular reactions of innate immunity Inflammation, the process in which phagocytic leukocytes are recruited and activated to kill microbes. Anti-viral defense, mediated by dendritic cells and NK cells.

  11. http://www.inflammationreliefguide.com/wp-content/uploads/2011/10/Inflammatory-Response.jpghttp://www.inflammationreliefguide.com/wp-content/uploads/2011/10/Inflammatory-Response.jpg

  12. http://dermatology-s10.cdlib.org/142/case_presentations/candidaglabrata/1.jpghttp://dermatology-s10.cdlib.org/142/case_presentations/candidaglabrata/1.jpg

  13. http://textbookofbacteriology.net/cellsindefenses75.jpg

  14. Innate vs Adaptive Immune Components There are also humoral vs cellular immune components

  15. http://www.mayoclinic.com/health/complete-blood-count/MY00476/DSECTION=resultshttp://www.mayoclinic.com/health/complete-blood-count/MY00476/DSECTION=results

  16. Granulocytes (or polymorphonuclears) • Neutrophils (or segs): 50 - 70% relative value (2500-7000 absolute value) • Eosinophils: 1 - 3% relative value (100-300 absolute value) • Basophils: 0.4% - 1% relative value (40-100 absolute value) • Agranulocytes(or mononuclears) • Lymphocytes: 25 - 35% relative value (1700-3500 absolute value) • Moncytes: 4 - 6% relative value (200-600 absolute value) • Eachdifferential always adds up to 100%. • To make an accurate assessment, consider both relative and absolute values. For example a relative value of 70% neutrophils may seem within normal limits; however, if the total WBC is 20,000, the absolute value (70% x 20,000) would be an abnormally high count of 14,000. http://www.rnceus.com/cbc/cbcwbc.html

  17. Leukocytes and epithelial cells that participate in innate immunity are capable of recognizing components of microbes that are shared among related microbes and are often essential for the infectivity of these pathogens. Recognition of PAMPs from different classes of microbial pathogens. Viruses, bacteria, fungi, and protozoa display several different PAMPs, some of which are shared between different classes of pathogens. Major PAMPs are nucleic acids, including DNA, dsRNA, ssRNA, and 5′-triphosphate RNA, as well as surface glycoproteins (GP), lipoproteins (LP), and membrane components (peptidoglycans [PG], lipoteichoic acid [LTA], LPS, and GPI anchors). These PAMPs are recognized by different families of PRRs.

  18. Recognition of PAMPs from different classes of microbial pathogens. Mogensen T H Clin. Microbiol. Rev. 2009;22:240-273

  19. http://www.pasteur.fr/ip/portal/action/WebdriveActionEvent/oid/01s-00003p-00ihttp://www.pasteur.fr/ip/portal/action/WebdriveActionEvent/oid/01s-00003p-00i

  20. How are Things Recognized • These microbial structures are called pathogen associated molecular patterns (PAMPs). • Leukocytes also recognize molecules released by injured and necrotic cells, which are sometimes called danger-associated molecular patterns (DAMPs). • The cellular receptors that recognize these molecules are often called pattern recognition receptors. • The best-defined pattern recognition receptors are a family of proteins called Toll-like receptors (TLRs) that are homologous to the Drosophila protein Toll.

  21. http://www.invitrogen.com/etc/medialib/en/images/ics_organized/applications/cell_tissue_analysis/data_diagram/750_wide.Par.59118.Image.750.810.1.gifhttp://www.invitrogen.com/etc/medialib/en/images/ics_organized/applications/cell_tissue_analysis/data_diagram/750_wide.Par.59118.Image.750.810.1.gif

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  23. TLRs are specific for components of different bacteria and viruses. TLRs are located on the cell surface and in endosomes, so they are able to recognize and initiate cellular responses to extracellular and ingested microbes. Upon recognition of microbes, the TLRs and other sensors signal by a common pathway that leads to the activation of transcription factors, notably NF-κB (nuclear factor κB). NF-κB turns on the production of cytokines and proteins that stimulate the microbicidal activities of various cells, notably the phagocytes. Other cellular receptors bind microbes for phagocytosis; these include receptors for mannose residues, which are typical of microbial but not host glycoproteins, and receptors for opsonins such as antibodies and complement proteins that coat microbes.

  24. Macrophages Macrophages are a part of the mononuclear phagocyte system. Macrophages that have phagocytosed microbes and protein antigens process the antigens and present peptide fragments to T cells. Thus, macrophages function as APCs in T-cell activation. Macrophages are key effector cells in certain forms of cell-mediated immunity, the reaction that serves to eliminate intracellular microbes. In this type of response, T cells activate macrophages and enhance their ability to kill ingested microbes. Macrophages also participate in the effector phase of humoral immunity. Macrophages efficiently phagocytose and destroy microbes that are opsonized (coated) by IgG or C3b. http://www.humpath.com/IMG/jpg/alveolar_macrophages_01_1-2.jpg

  25. Monocytes and neutrophils are phagocytes in the blood that can rapidly be recruited to any site of infection; monocytes that enter the tissues and mature are called macrophages.

  26. http://php.med.unsw.edu.au/cellbiology/images/a/a8/Endocytosis_types.pnghttp://php.med.unsw.edu.au/cellbiology/images/a/a8/Endocytosis_types.png

  27. http://iai.asm.org/content/80/4/1304/F1.large.jpg

  28. http://dc352.4shared.com/doc/-4JNWl_7/preview_html_m6a877314.jpghttp://dc352.4shared.com/doc/-4JNWl_7/preview_html_m6a877314.jpg

  29. http://classroom.sdmesa.edu/eschmid/f31-16_phagocytosis.jpg

  30. http://www.nature.com/nrmicro/journal/v7/n5/images/nrmicro2128-f2.jpghttp://www.nature.com/nrmicro/journal/v7/n5/images/nrmicro2128-f2.jpg

  31. Neutrophils are the first responders of the body's defense system. Neutrophils rapidly localize to areas of acute infection and phagocytize bacteria. Their cytoplasmic granules contain proteases and they are capable of generating reactive oxygen intermediates to kill the invading organism. Neutrophils are the most abundant white blood cell in circulation but they have a half life of only 1-2 days. http://upload.wikimedia.org/wikipedia/commons/2/29/Segmented_neutrophils.jpg

  32. http://www.nature.com/labinvest/journal/v80/n5/images/3780067f3.jpghttp://www.nature.com/labinvest/journal/v80/n5/images/3780067f3.jpg

  33. http://c431376.r76.cf2.rackcdn.com/38337/fimmu-03-00365-HTML/image_m/fimmu-03-00365-g001.jpghttp://c431376.r76.cf2.rackcdn.com/38337/fimmu-03-00365-HTML/image_m/fimmu-03-00365-g001.jpg

  34. http://www.rbej.com/content/figures/1477-7827-1-116-3.jpg

  35. http://edoc.hu-berlin.de/dissertationen/averhoff-petra-2006-05-24/HTML/image002.gifhttp://edoc.hu-berlin.de/dissertationen/averhoff-petra-2006-05-24/HTML/image002.gif

  36. http://www.elsevierimages.com/images/vpv/000/000/033/33679-0550x0475.jpghttp://www.elsevierimages.com/images/vpv/000/000/033/33679-0550x0475.jpg

  37. The proteins of the complement system, are some of the most important plasma proteins of the innate immune system. In innate immunity the complement system is activated by microbes using the alternative and lectin pathways; in adaptive immunity it is activated by antibodies using the classical pathway. http://www.bio.davidson.edu/courses/immunology/students/spring2006/finley/Imm%202-19.jpg

  38. http://www.profelis.org/amc/vorlesungen/gifs/MMPE_13IMM_163_02_eps.gifhttp://www.profelis.org/amc/vorlesungen/gifs/MMPE_13IMM_163_02_eps.gif

  39. http://ars.els-cdn.com/content/image/1-s2.0-S0145305X11000632-gr1.jpghttp://ars.els-cdn.com/content/image/1-s2.0-S0145305X11000632-gr1.jpg

  40. Natural Killer Cells NK cells are endowed with the ability to kill a variety of infected and tumor cells, without prior exposure to or activation by these microbes or tumors. This ability makes NK cells an early line of defense against viral infections and, perhaps, some tumors. CD16 is an Fc receptor for IgG, and it confers on NK cells the ability to lyse IgG-coated target cells. This phenomenon is known as antibody-dependent cell-mediated cytotoxicity (ADCC).

  41. http://weloveteaching.com/0bio105/lectures/systems/NK.gif

  42. The functional activity of NK cells is regulated by a balance between signals from activating and inhibitory receptors[10]. There are many types of activating receptors, of which the NKG2D family is the best characterized. The NKG2D receptors recognize surface molecules that are induced by various kinds of stress, such as infection and DNA damage. NK cell inhibitory receptors recognize self–class I MHC molecules, which are expressed on all healthy cells. The inhibitory receptors prevent NK cells from killing normal cells. Virus infection or neoplastic transformation often induces expression of ligands for activating receptors and at the same time reduces the expression of class I MHC molecules. As a result the balance is tilted toward activation, and the infected or tumor cell is killed

  43. http://ars.els-cdn.com/content/image/1-s2.0-S0264410X12000308-gr4.jpghttp://ars.els-cdn.com/content/image/1-s2.0-S0264410X12000308-gr4.jpg

  44. http://www.nature.com/nri/journal/v2/n10/images/nri911-f1.gifhttp://www.nature.com/nri/journal/v2/n10/images/nri911-f1.gif

  45. Major Histocompatibility Complex (MHC) Molecules: Peptide Display System of Adaptive Immunity MHC molecules were discovered as products of genes that evoke rejection of transplanted organs, and their name derives from the recognition that they are responsible for tissue compatibility between individuals.  The physiologic function of MHC molecules is to display peptide fragments of proteins for recognition by antigen-specific T cells. In humans the genes encoding the major histocompatibility molecules are clustered on a small segment of chromosome 6, the major histocompatibility complex, or the human leukocyte antigen (HLA) complex, so named because in humans MHC-encoded proteins were initially detected on leukocytes by the binding of antibodies. The HLA system is highly polymorphic, meaning that there are many alleles of each MHC gene in the population and each individual inherits one set of these alleles that is different from the alleles in most other individuals. This, as we see subsequently, constitutes a formidable barrier in organ transplantation. • .

  46. The virus-encoded proteins m04, m06 and m152 inhibit MHC class I expression on the surface of mouse cytomegalovirus (MCMV)-infected cells by a complex process that differs depending on the MHC class I alleles present in the host22. m04 can be expressed on the cell surface of MCMV-infected cells in a complex with MHC class I molecules; however, how this influences the recognition of MHC class I molecules by receptors on natural killer (NK) cells or T cells is unknown. Human cytomegalovirus (HCMV) also blocks the expression of MHC class I molecules in infected cells in an allele-specific manner (reviewed in Ref. 65). The HCMV proteins US2, US3, US10 and US11 interact with the MHC class I heavy chains on their own or with the heavy chains complexed with 2-microglobulin, ultimately resulting in their degradation, whereas US6 blocks TAP (transporter associated with antigen processing) function and UL83 inhibits protein entry into the proteasome. UL40 provides a leader peptide that binds to HLA-E allowing its expression on the surface of HCMV-infected cells, presumably for interactions with the inhibitory CD94–NKG2A (NK group 2, member A) receptor on NK cells. Both MCMV and HCMV inhibit expression of the NKG2D ligands in infected cells. The MCMV-encoded m152 protein targets RAE1 (retinoic acid early transcript 1), as well as MHC class I molecules, for degradation; m145 and m138 cooperate to prevent MULT1 (murine UL16-binding protein (ULBP)-like transcript 1) expression; and m138 and m155 cause degradation of H60. In humans, the HCMV-encoded UL16 protein inhibits expression of MICB (MHC-class-I-polypeptide-related sequence B), ULBP1, ULBP2 and RAET1G (retinoic-acid early transcript 1G), whereas UL142 prevents expression of MICA. Certain alleles of MICA, such as the common allele MICA*008, are resistant to downregulation by HMCV because of a truncation of the cytoplasmic domain. CD155, a ligand for the activating NK-cell receptors DNAM1 (DNAX adhesion molecule 1) and CD96, is targeted by UL141. http://www.nature.com/nri/journal/v8/n4/fig_tab/nri2276_F2.html

  47. Activation of B and T lymphocytes Naive Plasma cells Naive The innate immune system provides immediate protection. The adaptive response takes time to develop and is antigen specific.

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