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PMID: 10915094 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Persistence of human papillomavirus type 16 infection is associated with lack of cytotoxic T lymphocyte response to the E6 antigens.

The Journal of infectious diseases ·Vol. 182 ·No. 2 ·2000-08-00 ·Pages 595-8

Nakagawa M, Stites DP, Patel S, Farhat S, Scott M, Hills NK, Palefsky JM, Moscicki AB

Abstract

Our cross-sectional study suggested that cytotoxic T lymphocyte (CTL) responses have a protective effect in squamous intraepithelial lesion (SIL) development. More CTL responses in women with human papillomavirus type 16 (HPV 16) infection without SILs than with SILs were detected. In the current longitudinal study, the role of CTL in clearing HPV 16 infection in women without SILs was investigated. Women with HPV 16 infection (n=51) were enrolled, along with HPV 16-negative control women (n=3). Twenty-two (55%) of 40 women who cleared HPV 16 infection had an E6 CTL response at least once, compared with none of 9 women who had HPV 16 persistence (P=.003). Such a difference was not demonstrated for E7; 25 (63%) of 40 women who cleared HPV 16 infection responded, versus 5 (56%) of 9 women with persistence (P=.720). It appears that lack of response to E6 is important in the persistence of HPV 16 infection.

MeSH Terms
Adolescent Adult Cohort Studies Female Humans Oncogene Proteins, Viral/immunology Papillomaviridae/immunology,isolation & purification Papillomavirus Infections/immunology Repressor Proteins T-Lymphocytes, Cytotoxic/immunology Tumor Virus Infections/immunology
Chemicals
E6 protein, Human papillomavirus type 16 Oncogene Proteins, Viral Repressor Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Nakagawa M
Dept. of Laboratory Medicine, School of Medicine, University of California at San Francisco, San Francisco, CA 94143-0134, USA.
Stites D P
Patel S
Farhat S
Scott M
Hills N K
Palefsky J M
Moscicki A B
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
0022-1899
Published
2000-08-00
Epub
2000-00-28
Pages
595-8
Language
English
Region
United States
NLM ID
0413675
Subset
IM
Grants
NCI NIH HHS · R37 CA051323 · United States
NCI NIH HHS · CA51323 · United States
NCI NIH HHS · CA75974 · United States
NCRR NIH HHS · M01RR01271 · United States
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