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Infection and Immunity, March 2000, p. 1719-1723, Vol. 68, No. 3
Laboratory of Genetics, University of
Wisconsin,1 and Departments of
Medicine,2 Medical Microbiology and
Immunology,3 and
Pathology,4 University of Wisconsin
Medical School, Madison, Wisconsin 53706
Received 3 August 1999/Returned for modification 24 September
1999/Accepted 23 November 1999
We previously identified 18 stimulatory Chlamydia
trachomatis major outer membrane protein (MOMP) peptides
containing at least 23 epitopes presented with various HLA class II
allotypes. Only one peptide contained an epitope localized in a
variable segment (VS2). Continued studies reported here identified a
total of five VS peptides containing T-cell epitopes that are
distributed among MOMPs VS1, VS2, and VS4. Only MOMP-primed T-cell
cultures from subjects infected with serovar E responded to the serovar
E VS peptides, while the response of such cultures to constant-segment peptides was independent of the infecting serovar. Furthermore, MOMP-primed T cells proliferated in response only to the VS peptides encoded in serovar E but not to the corresponding peptides derived from
serovar F, I, or J, confirming that these responses were serovar specific.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
T-Cell Epitopes in Variable Segments of
Chlamydia trachomatis Major Outer Membrane Protein Elicit
Serovar-Specific Immune Responses in Infected Humans
*
Corresponding author. Present address for Linette
Ortiz: Department of Pharmacology, Rm. 3635 MSC, University of
Wisconsin, 1300 University Ave., Madison, WI 53706. Phone: (608)
265-0795. Fax: (608) 262-1257. E-mail:
lortiz{at}facstaff.wisc.edu. Mailing address for Robert
DeMars: Laboratory of Genetics, University of Wisconsin, 445 Henry
Mall, Madison, WI 53706. Phone: (608) 262-3402. Fax: (608) 262-2976. E-mail: ridemars{at}facstaff.wisc.edu.
This is paper 3491 from the Laboratory of Genetics, University of
Wisconsin-Madison.
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