CBA/J mice generate protective immunity to soluble Ag85 but fail to respond efficiently to Ag85 during natural Mycobacterium tuberculosis infection
Author:
Affiliation:
1. Center for Microbial Interface Biology; The Ohio State University; Columbus; OH; USA
2. Vanderbilt Vaccine Center; Vanderbilt University; Nashville; TN; USA
3. Department of Veterinary Biosciences; The Ohio State University; Columbus; OH; USA
Publisher
Wiley
Subject
Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/eji.201142054/fullpdf
Reference46 articles.
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2. Pathology of post primary tuberculosis of the lung: an illustrated critical review;Hunter;Tuberculosis,2011
3. Isolation and analysis of circulating tuberculous antigens in Mycobacterium tuberculosis;Shende;Indian J. Tuberc,2007
4. Specific lymphoproliferation, gamma interferon production, and serum immunoglobulin G directed against a purified 32 kDa mycobacterial protein antigen (P32) in patients with active tuberculosis;Huygen;Scand. J. Immunol,1988
5. T-cell recognition of Mycobacterium tuberculosis culture filtrate fractions in tuberculosis patients and their household contacts;Demissie;Infect. Immun,1999
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