Class II MHC function in macrophages and mice infected with mycobacterium

Bibliographic Details
Main Author: Nepal, Rajeev Mani
Language:English
Published: The Ohio State University / OhioLINK 2006
Subjects:
DM
Online Access:http://rave.ohiolink.edu/etdc/view?acc_num=osu1141761508
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spelling ndltd-OhioLink-oai-etd.ohiolink.edu-osu11417615082021-08-03T05:50:47Z Class II MHC function in macrophages and mice infected with mycobacterium Nepal, Rajeev Mani Class II MHC Mycobacteria Mycobacterium tuberculosis Mycobacterium avium Cathepsin Cathepsin L DM Macrophage GMCSF M-CSF Stability Class II MHC The interaction between macrophages and CD4+ T cells is central to the adaptive immune response against Mycobacterium tuberculosis (MTB). The primary goal of this thesis was to determine if macrophages infected with pathogenic Mycobacterium spp can function in the processing and presentation of antigens via the class II MHC pathway. To this end, we first characterized the endocytic proteases available to the infected macrophage. We found that the maturation of Cat L into its' two-chain active forms is impaired in macrophages harboring either M. avium or M. tuberculosis, rendering these cells deficient in the predominant intracellular, and extracellular active forms of the enzyme. Secondly, we showed that DM, but not Cat B, -S, or -L, is absolutely required to control a primary aeorosl infection of mice with MTB. MTB specific CD4+ T cells were not elicited in the absence of DM. The data suggest that most, if not all MTB antigens require DM for presentation by class II molecules to CD4+ T cells. Thirdly, we demonstrated that macrophages of distinct lineages and activation states differ in the ability to process and present mycobacteria derived antigens via class II MHC molecules. The data showed that GM-CSF derived bone marrow macrophages were significantly more efficient than M-CSF derived bone marrow macrophages at processing M. avium and M. tuberulosis bacilli (live or dead) for presentation of the immunodominant anigen, Ag85B, to specific T cells. The varying ability of each cell type to function in antigen presentation when infected may contribute to the ability of mycobacteria to persist in the host. Finally, we showed that the phagocytosis of M. avium by macrophages result in the generation of more stable nascent class II-peptide complexes at the cell surface, that are capable of stimulating antigen specific CD4+ T cells for prolonged periods. 2006-03-15 English text The Ohio State University / OhioLINK http://rave.ohiolink.edu/etdc/view?acc_num=osu1141761508 http://rave.ohiolink.edu/etdc/view?acc_num=osu1141761508 unrestricted This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
collection NDLTD
language English
sources NDLTD
topic Class II MHC
Mycobacteria
Mycobacterium tuberculosis
Mycobacterium avium
Cathepsin
Cathepsin L
DM
Macrophage
GMCSF
M-CSF
Stability Class II MHC
spellingShingle Class II MHC
Mycobacteria
Mycobacterium tuberculosis
Mycobacterium avium
Cathepsin
Cathepsin L
DM
Macrophage
GMCSF
M-CSF
Stability Class II MHC
Nepal, Rajeev Mani
Class II MHC function in macrophages and mice infected with mycobacterium
author Nepal, Rajeev Mani
author_facet Nepal, Rajeev Mani
author_sort Nepal, Rajeev Mani
title Class II MHC function in macrophages and mice infected with mycobacterium
title_short Class II MHC function in macrophages and mice infected with mycobacterium
title_full Class II MHC function in macrophages and mice infected with mycobacterium
title_fullStr Class II MHC function in macrophages and mice infected with mycobacterium
title_full_unstemmed Class II MHC function in macrophages and mice infected with mycobacterium
title_sort class ii mhc function in macrophages and mice infected with mycobacterium
publisher The Ohio State University / OhioLINK
publishDate 2006
url http://rave.ohiolink.edu/etdc/view?acc_num=osu1141761508
work_keys_str_mv AT nepalrajeevmani classiimhcfunctioninmacrophagesandmiceinfectedwithmycobacterium
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