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PMID: 11309137 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

CD1d-restricted NK T cells are dispensable for specific antibody responses and protective immunity against liver stage malaria infection in mice.

Parasite immunology ·Vol. 23 ·No. 5 ·2001-05-00 ·Pages 267-9

Romero JF, Eberl G, MacDonald HR, Corradin G

Abstract

Immunization with a single dose of irradiated sporozoites is sufficient to induce protection against malaria in wild-type mice. Although this protection is classically attributed to conventional CD4+ and CD8+ T cells, several recent reports have suggested an important role for CD1-restricted NK T cells in immunity to malaria. In this study, we directly compared the ability of C57BL/6 wild-type and CD1-deficient mice to mount a protective immune response against Plasmodium berghei sporozoites. Our data indicate that CD1-restricted NK T cells are not required for protection in this model system. Moreover, specific IgG antibody responses to the P. berghei circumsporozoite repeat sequence were also unaffected by CD1 deficiency. Collectively, our data demonstrate that CD1-restricted NK T cells are dispensable for protective immunity to liver stage P. berghei infection.

MeSH Terms
Animals Antibodies, Protozoan/immunology Antigens, CD1/immunology Antigens, CD1d Disease Models, Animal Female Interleukin-12/immunology Killer Cells, Natural/immunology Liver/immunology Malaria/immunology Male Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Knockout Plasmodium berghei/immunology T-Lymphocytes/immunology
Chemicals
Antibodies, Protozoan Antigens, CD1 Antigens, CD1d Interleukin-12
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Romero J F
Institute of Biochemistry, Lausanne Branch, University of Lausanne, CH-1066 Epalinges, Switzerland.
Eberl G
MacDonald H R
Corradin G
Article Info
Journal
Parasite immunology
Abbr.
Parasite Immunol
ISSN
0141-9838
Published
2001-05-00
Pages
267-9
Language
English
Region
England
NLM ID
7910948
Subset
IM
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