Association ofChlamydia trachomatisHeat‐Shock Protein 60 Antibody and HLA Class II DQ Alleles
Author(s) -
Lakshmi K. Gaur,
Rosanna W. Peeling,
Mary Cheang,
Joshua Kimani,
J Bwayo,
Frank Plummer,
Robert C. Brunham
Publication year - 1999
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314838
Subject(s) - chlamydia trachomatis , chlamydia , antibody , allele , immunology , human leukocyte antigen , biology , chlamydiaceae , genotype , pelvic inflammatory disease , virology , polymerase chain reaction , antigen , medicine , genetics , gene , gynecology
A total of 113 female commercial sex workers had individual alleles for HLA class II genes determined by using labeled sequence-specific oligonucleotide probes to hybridize to polymerase chain reaction products of amplified DNA. Women also had microimmunofluorescent (MIF) antibody titers to Chlamydia trachomatis elementary bodies and ELISA antibody to recombinant chlamydial heat-shock protein 60 (Chsp60) determined. Women were prospectively followed at monthly intervals over 2 years for incident C. trachomatis infection and acute pelvic inflammatory disease (PID). HLA DQA1*0401 and DQB1*0402 alleles were statistically associated with increased prevalence and amount of antibody to Chsp60 but not MIF antibody. However, these alleles did not alter the risk for chlamydial PID. The potential role that HLA DQ may play in chlamydial disease pathogenesis requires further study.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom