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Infection and Immunity, January 2001, p. 89-96, Vol. 69, No. 1
0019-9567/01/$04.00+0   DOI: 10.1128/IAI.69.1.89-96.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

In Vitro Responsiveness of gamma delta T Cells from Mycobacterium bovis-Infected Cattle to Mycobacterial Antigens: Predominant Involvement of WC1+ Cells

Allister J. Smyth,1 Michael D. Welsh,2,* R. Martyn Girvin,2 and John M. Pollock2

Department of Veterinary Science, The Queen's University of Belfast,1 and Veterinary Sciences Division, The Department of Agriculture and Rural Development,2 Stormont, Belfast BT4 3SD, United Kingdom

Received 20 March 2000/Returned for modification 15 May 2000/Accepted 27 September 2000

It is generally accepted that protective immunity against tuberculosis is generated through the cell-mediated immune (CMI) system, and a greater understanding of such responses is required if better vaccines and diagnostic tests are to be developed. gamma delta T cells form a major proportion of the peripheral blood mononuclear cells (PBMC) in the ruminant system and, considering data from other species, may have a significant role in CMI responses in bovine tuberculosis. This study compared the in vitro responses of alpha beta and gamma delta T cells from Mycobacterium bovis-infected and uninfected cattle. The results showed that, following 24 h of culture of PBMC with M. bovis-derived antigens, the majority of gamma delta T cells from infected animals became highly activated (upregulation of interleukin-2R), while a lower proportion of the alpha beta T-cell population showed activation. Similar responses were evident to a lesser degree in uninfected animals. Study of the kinetics of this response showed that gamma delta T cells remained significantly activated for at least 7 days in culture, while activation of alpha beta T cells declined during that period. Subsequent analysis revealed that the majority of activated gamma delta T cells expressed WC1, a 215-kDa surface molecule which is not expressed on human or murine gamma delta T cells. Furthermore, in comparison with what was found for CD4+ T cells, M. bovis antigen was found to induce strong cellular proliferation but relatively little gamma interferon release by purified WC1+ gamma delta T cells. Overall, while the role of these cells in protective immunity remains unclear, their highly activated status in response to M. bovis suggests an important role in antimycobacterial immunity, and the ability of gamma delta T cells to influence other immune cell functions remains to be elucidated, particularly in relation to CMI-based diagnostic tests.


* Corresponding author. Mailing address: Department of Bacteriology, Veterinary Sciences Division, The Department of Agriculture and Rural Development, Stoney Road, Stormont, Belfast BT4 3SD, United Kingdom. Phone: 028 90 525642. Fax: 028 90 525745. E-mail: michael.welsh{at}dardni.gov.uk.


Infection and Immunity, January 2001, p. 89-96, Vol. 69, No. 1
0019-9567/01/$04.00+0   DOI: 10.1128/IAI.69.1.89-96.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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