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Infection and Immunity, January 1999, p. 57-63, Vol. 67, No. 1
Department of Molecular Microbiology and
Immunology, Johns Hopkins University School of Hygiene and Public
Health, Baltimore, Maryland 21205
Received 22 June 1998/Returned for modification 3 August
1998/Accepted 7 October 1998
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Murine

T Lymphocytes Elicited during
Plasmodium yoelii Infection Respond to Plasmodium
Heat Shock Proteins

T cells accumulate during Plasmodium infections
in both murine and human malarias. The biological role of these cells
and the antigens that they recognize are not clearly understood,
although recent findings indicate that 
T cells in general
influence both innate and antigen-specific adaptive host responses. We
examined the accumulation of 
T cells elicited during infection
with virulent and avirulent Plasmodium yoelii parasites in
relatively susceptible and resistant strains of mice. Our results
indicated that in nonlethal malaria infections, 
T cells comprise
a larger proportion of splenic T cells than in lethal infections and
that only a live infection is capable of inducing an increase in the percentage of 
T cells in vivo. Furthermore, we demonstrate that

T cells elicited during a P. yoelii infection
respond by proliferation in vitro to P. falciparum heat
shock proteins (HSPs) of 60 and 70 kDa, suggesting a possible
immunological involvement of parasite HSPs in this arm of the cellular
immune response during malarial infection in mice.
*
Corresponding author. Mailing address: Department of
Molecular Microbiology and Immunology, Johns Hopkins University School of Hygiene and Public Health, 615 N. Wolfe St., Baltimore, MD 21205. Phone: (410) 955-7177. Fax: (410) 955-0105. E-mail:
nkumar{at}jhsph.edu.
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