Immune privilege

Certain sites of the human body have immune privilege, meaning they are able to tolerate the introduction of antigens without eliciting an inflammatory immune response. Tissue grafts are normally recognised as foreign antigen by the body and attacked by the immune system. However in immune privileged sites, tissue grafts can survive for extended periods of time without rejection occurring.[1] Immunologically privileged sites were thought to include:

Immune privilege is also believed to occur to some extent, or able to be induced, in articular cartilage.[3][4][5]

Immune privilege is thought to be an evolutionary adaptation to protect vital structures from the potentially damaging effects of an inflammatory immune response. Inflammation in the brain or eye can lead to loss of organ function, while immune responses directed against a fetus can lead to the loss of the fetus.

Medically, a cornea transplant takes advantage of this, as does knee meniscal transplantation.

Mechanisms

Antigens from immune privileged regions have been found to interact with T cells in an unusual way inducing tolerance as previously opposed to a destructive response.[6] Immune privilege has emerged as an active rather than a passive process.

Physical structures surrounding privileged sites cause a lack of lymphatic drainage, limiting the immune system's ability to enter the site. Other factors that contribute to the maintenance of immune privilege include:

The nature of isolation of immunologically privileged sites from the rest of the body's immune system can cause them to become targets of autoimmune diseases or conditions, including sympathetic ophthalmia in the eye.

Immunologically privileged sites

Eye

Main article: Ocular immune system

As well as the mechanisms that limit immune cell entry and induce immune suppression, the eye also contains active immune cells that act upon the detection of foreign antigens. These cells interact with the immune system to induce unusual suppression of the systemic immune system response to an antigen introduced into the eye. This is known as Anterior Chamber Associated Immune Deviation (ACAID).[9][10]

Sympathetic ophthalmia is a rare disease which results from the isolation of the eye from the systemic immune system. Usually, trauma to one eye induces the release of eye antigens which are recognized and picked up by local antigen presenting cells (APC) such as macrophages and dendritic cells. These APC carry the antigen to local lymph nodes to be sampled by T cells and B cells. Entering the systemic immune system, these antigens are recognized as foreign and an immune response is mounted against them. The result is the sensitization of immune cells against a self-protein, causing an autoimmune attack on both the damaged eye and the non-damaged eye.[6]

In this manner, the immune-privileged property has served to work against the eye instead. T cells normally encounter self-antigens during their development, when they move to the tissue draining lymph nodes. Anergy is induced in T cells which bind to self-antigens, deactivating them and preventing an autoimmune response in the future. However, the physical isolation of eye antigens results in the body's T cells never having encountered them at any time during development. Studies in mice have shown that the lack of presentation of eye self-antigens to specific T cells will fail to induce a sufficient amount of anergy to the self-antigens. While the lack of antigen presentation (due to the physical barriers) is sufficient to prevent the activation of autoreactive immune cells to the eye, the failure to induce sufficient anergy to T cells has detrimental results. In the case of damage or chance presentation to the immune system, the antigen presentation and immune response will occur at elevated rates.[11]

Placenta and Fetus

The mother’s immune system is able to provide protection from microbial infections without mounting an immune response against fetal tissues expressing paternally inherited alloantigens. A better understanding of the immunology of pregnancy may lead to the discovery of reasons for miscarriage.

Regulatory T cells (Tregs) appear to be important in the maintenance of tolerance to fetal antigen. Increased numbers of Tregs are found during normal pregnancy. In both mouse models and humans diminished numbers of Tregs were associated with immunological rejection of the fetus and miscarriage. Experiments in mice involving the transfer of CD4+/CD25+ Treg cells from normal pregnant mice into abortion-prone animals resulted in the prevention of abortion.[12] This confirmed the importance of these cells in maintaining immune privilege in the womb.

A number of theories exist as to the exact mechanism by which fetal tolerance is maintained. It has been proposed in recent literature[13] that a tolerant microenvironment is created at the interface between the mother and fetus by regulatory T-cells producing "tolerant molecules". These molecules including heme oxygenase 1 (HO-1), leukaemia inhibitory factor (LIF), transforming growth factor β (TGF-β) and interleukin 10 (IL-10) have all been implicated in the induction of immune tolerance. Foxp3 and neuropillin are markers expressed by the regulatory T-cells by which they are identified.

Testes

Main article: Testicular immunology

Sperm are immunogenic - that is they will cause an autoimmune reaction if transplanted from the testis into a different part of the body. This has been demonstrated in experiments using rats by Lansteiner (1899) and Metchinikoff (1900),[14][15] mice [16] and guinea pigs.[17] The likely reason for this is that sperm first mature at puberty, after immune tolerance is established, therefore the body recognizes them as foreign and mounts an immune reaction against them. Therefore, mechanisms for their protection must exist in this organ to prevent any autoimmune reaction. The blood-testis barrier is likely to contribute to the survival of sperm. However, it is believed in the field of testicular immunology that the blood-testis barrier cannot account for all immune suppression in the testis, due to (1) its incompleteness at a region called the rete testis [15] and (2) the presence of immunogenic molecules outside the blood-testis barrier, on the surface of spermatogonia.[14][15] Another mechanism which is likely to protect sperm is the suppression of immune responses in the testis.[18][19]

Central Nervous System

The Central Nervous System (CNS), which includes the brain and spinal cord, is a sensitive system with limited capacity for regeneration. In that regard, the concept of "immune privilege" within the CNS was once thought to be critical in limiting inflammation. The blood–brain barrier plays an important role in maintaining the separation of CNS from the systemic immune system but the presence of the blood–brain barrier, does not, on its own, provide immune privilege.[20] It is thought that immune privilege within the CNS varies throughout the different compartments of the system, being most pronounced in the parenchyma tissue or "white matter".[20]

The concept of CNS as an "immune-privileged" organ system, however, has been overwhelmingly challenged and re-evaluated over the last two decades. Current data do not only indicate the presence of resident CNS macrophages (known as microglia) within the CNS, but there is also a wide body of evidence suggesting the active interaction of the CNS with peripheral immune cells.[21]

Generally, in normal (uninjured) tissue, antigens are taken up by antigen presenting cells (dendritic cells), and subsequently transported to the lymph nodes. Alternatively, soluble antigens can drain into the lymph nodes. In contrast, in the CNS, dendritic cells are not thought to be present in normal parenchymal tissue or perivascular space although they are present in the meninges and choroids plexus.[20] Thus, the CNS is thought to be limited in its capacity to deliver antigens to local lymph nodes and cause T-cell activation.[22]

Although there is no conventional lymphatic system in the CNS, the drainage of antigens from CNS tissue into the cervical lymph nodes has been demonstrated. The response elicited in the lymph nodes to CNS antigens is skewed towards B-cells. Dendritic cells from cerebrospinal fluid have been found to migrate to B-cell follicles of cervical lymph nodes.[23] The skewing of the response to antigen from the CNS towards a humoral response means that a more dangerous inflammatory T-cell response can be avoided.

The induction of systemic tolerance to an antigen introduced into the CNS has been previously shown.[24] This was seen in the absence of the T-cell mediated inflammatory "delayed type hypersensitivity reaction" (DTH) when the antigen was reintroduced in another part of the body. This response is analogous to ACAID in the eye.

History of research

The existence of immune privileged regions of the eye was recognised as early as the late 19th century and investigated by Medawar. The original explanation of this phenomenon was that physical barriers around the immune privileged site enabled it to avoid detection from the immune system altogether, preventing the immune system from responding to any antigens present. More recent investigations have revealed a number of different mechanisms by which immune privileged sites interact with the immune system.

References

  1. ↑ 1.0 1.1 Hong Seokmann, Kaer Van, Luc (1999). "Immune Privilege: Keeping an Eye on Natural Killer T Cells". The Journal of Experimental Medicine 190 (9): 1197–1200.
  2. ↑ Ziv, Y.et al (2006). Nature Neuroscience, Immune cells contribute to the maintenance of neurogenesis and spatial learning abilities in adulthood 9, 268 - 275.
  3. ↑ Sun Z1, Zhang M, Zhao XH, Liu ZH, Gao Y, Samartzis D, Wang HQ, Luo ZJ (2013). "Immune cascades in human intervertebral disc: the pros and cons". International Journal of Clinical and Experimental Medicine 6 (6): 1009–1014. PMC 3657352. PMID 23696917.
  4. ↑ Fujihara Y1, Takato T, Hoshi K (2014). "Macrophage-inducing FasL on chondrocytes forms immune privilege in cartilage tissue engineering, enhancing in vivo regeneration". STEM CELLS 32 (2): 1208–1219. doi:10.1002/stem.1636. PMID 24446149.
  5. ↑ Abazari A1, Jomha NM, Elliott JA, McGann LE (2013). "Cryopreservation of articular cartilage". CRYOBIOLOGY 66 (3): 201–209. doi:10.1016/j.cryobiol.2013.03.001. PMID 23499618.
  6. ↑ 6.0 6.1 Janeway, C. A.Jr., Travers, P., Walport, M., Shlomchik. M.J. (2005). ImmunoBiology, the immune system in health and disease 6th Edition. Garland Science.
  7. ↑ "Autoimmunity". webMIC 419: Immunology. University of Arizona.
  8. ↑ Green DR, Ware CF (June 1997). "Fas-ligand: privilege and peril". Proc Natl Acad Sci USA. 94 (12): 5986–90. doi:10.1073/pnas.94.12.5986. PMC 33671. PMID 9177153.
  9. ↑ Keino, H, Takeuchi, M, Kezuka, T, Hattori, T, Usui, M, Taguchi, O, Streilein, JW, Stein-Streilein, J. (2006). Induction of Eye-Derived Tolerance Does Not Depend on Naturally Occurring CD4+CD25+ T Regulatory Cells. Investigative Ophthalmology and Visual Science.47:1047-1055
  10. ↑ Streilein, JW, Stein-Streilein, J. (2002). Anterior chamber associated immune deviation (ACAID): regulation, biological relevance, and implications for therapy. International Reviews of Immunology. 21(2-3):123-52
  11. ↑ Lambe, T., J. C. H. Leung, H. Ferry, T. Bouriez-Jones, K. Makinen, T. L. Crockford, H. R. Jiang, J. M. Nickerson, L. Peltonen, J. V. Forrester, and R. J. Cornall. (2007). Limited Peripheral T Cell Anergy Predisposes to Retinal Autoimmunity. The Journal of Immunology 178:4276-4283.
  12. ↑ Zenclussen A,C. (2006). Regulatory T cells in pregnancy. Springer Seminars in Immunopathology. 28(1): 31-39
  13. ↑ Zenclussen AC, Schumacher A, Zencluseen ML, Wafula P, Volk HD. (2007). Immunology of pregnancy: cellular mechanisms allowing fetal survival within the maternal uterus. Expert Reviews in Molecular Medicine. 9 (10):1-14.
  14. ↑ 14.0 14.1 Hedger MP, Hales DB (2006). "Immunophysiology of the Male Reproductive Tract". In Neill JD. Knobil and Neill's Physiology of Reproduction. Elsevier. pp. 1195–1286. ISBN 0-12-515401-1.
  15. ↑ 15.0 15.1 15.2 Fijak M, Meinhardt A (2006). "The testis in immune privilege.". Immunol Rev. 213 (1): 66–81. doi:10.1111/j.1600-065X.2006.00438.x. PMID 16972897.
  16. ↑ Kohno S, Munoz JA, Williams TM, Teuscher C, Bernard CC, Tung KS. (1983). "Immunopathology of murine experimental allergic orchitis.". J Immunol. 130 (6): 2675–2682. PMID 6682874.
  17. ↑ Teuscher C, Wild GC, Tung KS (1982). "Immunochemical analysis of guinea pig sperm autoantigens.". Biol reprod. 26 (2): 218–229. doi:10.1095/biolreprod26.2.218. PMID 7039703.
  18. ↑ Kern S, Robertson SA, Mau VJ, Maddocks S (1995). "Cytokine secretion by macrophages in the rat testis.". Biol Reprod. 53 (6): 1407–1416. doi:10.1095/biolreprod53.6.1407. PMID 8562698.
  19. ↑ O'Bryan MK, Gerdprasert O, Nikolic-Paterson DJ, Meinhardt A, Muir JA, Foulds LM, Phillips DJ, de Kretser DM, Hedger MP (2005). "Cytokine profiles in the testes of rats treated with lipopolysaccharide reveal localized suppression of inflammatory responses.". Am J Physiol Regul Integr Comp Physiol. 288 (6): R1744–R1755. doi:10.1152/ajpregu.00651.2004. PMID 15661966.
  20. ↑ 20.0 20.1 20.2 Galea I, Beckmann I, Perry V.H. (2007). What is Immune Privilege (not)?. Trends in Immunology. 28(1): 12-18
  21. ↑ Carson MJ, Doose JM, Melchior B, Schmid CD, Ploix CC (October 2006). "CNS immune privilege: hiding in plain sight". Immunol. Rev. 213 (1): 48–65. doi:10.1111/j.1600-065X.2006.00441.x. PMC 2633103. PMID 16972896.
  22. ↑ Mendez-Fernandez Y.V. et al. (2005). "Anatomical and cellular requirements for the activation and migration of virus-specific CD8+ T cells to the brain during Theiler's virus infection". Journal of Virology 79: 3063–3070. doi:10.1128/jvi.79.5.3063-3070.2005.
  23. ↑ Hatterer E. et al. (2006). "How to drain without lymphatics? Dendritic cells migrate from the cerebrospinal fluid to the B-cell follicles of cervical lymph nodes". Blood 107: 806–812. doi:10.1182/blood-2005-01-0154.
  24. ↑ Wenkel H. et al. (2000). "Systemic immune deviation in the CNS does not necessarily depend on the integrity of the blood–brain barrier". Journal of Immunology 164: 5125–5131. doi:10.4049/jimmunol.164.10.5125.