Human pathogen subversion of antigen presentation
- PMID: 10399076
- DOI: 10.1111/j.1600-065x.1999.tb01294.x
Human pathogen subversion of antigen presentation
Abstract
Many pathogens have co-evolved with their human hosts to develop strategies for immune evasion that involve disruption of the intracellular pathways by which antigens are bound by class I and class II molecules of the major histocompatibility complex (MHC) for presentation to T cells. Here the molecular events in these pathways are reviewed and pathogen interference is documented for viruses, extracellular and intracellular bacteria and intracellular parasites. In addition to a general review, data from our studies of adenovirus, Chlamydia trachomatis and Coxiella burnetii are summarized. Adenovirus E19 is the first viral gene product described that affects class I MHC molecule expression by two separate mechanisms, intracellular retention of the class I heavy chain by direct binding and by binding to the TAP transporter involved in class I peptide loading. Coxiella and Chlamydia both affect peptide presentation by class II MHC molecules as a result of their residence in endocytic compartments, although the properties of the parasitophorous vacuoles they form are quite different. These examples of active interference with antigen presentation by viral gene products and passive interference by rickettsiae and bacteria are typical of the strategies used by these different classes of pathogens, which need to evade different types of immune responses. Pathogen-host co-evolution is evident in these subversion tactics for which the pathogen crime seems tailored to fit the immune system punishment.
Similar articles
-
MHC presentation via autophagy and how viruses escape from it.Semin Immunopathol. 2010 Dec;32(4):373-81. doi: 10.1007/s00281-010-0227-7. Epub 2010 Sep 21. Semin Immunopathol. 2010. PMID: 20857294 Review.
-
Viral interference with MHC class I antigen presentation pathway: the battle continues.Vet Immunol Immunopathol. 2005 Aug 15;107(1-2):1-15. doi: 10.1016/j.vetimm.2005.04.006. Vet Immunol Immunopathol. 2005. PMID: 15978672 Review.
-
Viral strategies of immune evasion.Science. 1998 Apr 10;280(5361):248-53. doi: 10.1126/science.280.5361.248. Science. 1998. PMID: 9535648 Review.
-
Pathogen evasion strategies for the major histocompatibility complex class I assembly pathway.Immunology. 2008 May;124(1):1-12. doi: 10.1111/j.1365-2567.2008.02804.x. Epub 2008 Feb 18. Immunology. 2008. PMID: 18284468 Free PMC article. Review.
-
Both Major Histocompatibility Complex Class I (MHC-I) and MHC-II Molecules Are Required, while MHC-I Appears To Play a Critical Role in Host Defense against Primary Coxiella burnetii Infection.Infect Immun. 2018 Mar 22;86(4):e00602-17. doi: 10.1128/IAI.00602-17. Print 2018 Apr. Infect Immun. 2018. PMID: 29311245 Free PMC article.
Cited by
-
Roles for Pathogen Interference in Influenza Vaccination, with Implications to Vaccine Effectiveness (VE) and Attribution of Influenza Deaths.Infect Dis Rep. 2022 Sep 23;14(5):710-758. doi: 10.3390/idr14050076. Infect Dis Rep. 2022. PMID: 36286197 Free PMC article. Review.
-
MHC I-dependent antigen presentation is inhibited by poliovirus protein 3A.Proc Natl Acad Sci U S A. 2000 Dec 5;97(25):13790-5. doi: 10.1073/pnas.250483097. Proc Natl Acad Sci U S A. 2000. PMID: 11095746 Free PMC article.
-
Chlamydia trachomatis-infected epithelial cells and fibroblasts retain the ability to express surface-presented major histocompatibility complex class I molecules.Infect Immun. 2014 Mar;82(3):993-1006. doi: 10.1128/IAI.01473-13. Epub 2013 Dec 16. Infect Immun. 2014. PMID: 24343651 Free PMC article.
-
Coxiella burnetii Epitope-Specific T-Cell Responses in Patients with Chronic Q Fever.Infect Immun. 2019 Sep 19;87(10):e00213-19. doi: 10.1128/IAI.00213-19. Print 2019 Oct. Infect Immun. 2019. PMID: 31331958 Free PMC article.
-
[Renal cell carcinoma associated proteins. Isolation, cloning and immunogenicity evaluation].Urologe A. 2007 Sep;46(9):1292-8. doi: 10.1007/s00120-007-1418-2. Urologe A. 2007. PMID: 17628779 German. No abstract available.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous