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single-cell cytokine analysis allows detection of cervical T-cell responses against human papillomavirus type 16 L1 in women infected with genital HPV

✍ Scribed by Jo-Ann S. Passmore; Vanessa C. Burch; Enid G. Shephard; Dianne J. Marais; Bruce Allan; Patti Kay; Robert C. Rose; Anna-Lise Williamson


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
115 KB
Volume
67
Category
Article
ISSN
0146-6615

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✦ Synopsis


Abstract

Specific types of human papillomavirus (HPV) are known to play a causal role in the development of cervical cancer, with human papillomavirus type 16 (HPV‐16) identified as the predominant type. Despite this, little is known about cervical immune responses to this pathogen. The aim of this study was to assess the feasibility of cervical cytobrush sampling and single‐cell cytokine staining to investigate cervical lymphocyte‐specific cytokine responses to HPV‐16 antigens. Of eighteen women recruited into the study, five were HPV DNA positive at the cervix (current exposure) and a further five had circulating antibodies to HPV‐16 (previous exposure). Cervical lymphocytes, isolated from the five HPV DNA‐positive women, two HPV DNA‐negative controls, and one woman with circulating HPV‐16 antibodies were assessed for HPV‐specific responses using intracellular staining for interferon‐γ (IFN‐γ) and interleukin‐4 (IL‐4). We demonstrate that both CD4^+^ and CD8^+^ cervical T lymphocytes, harvested from noninfected and infected subjects, produce these cytokines in response to nonspecific stimulation. However, antigen‐specific (HPV‐16 L1) IFN‐γ production by CD4^+^ and CD8^+^ cervical T lymphocytes is only detectable in women exposed currently or previously to HPV‐16. This is the first time that antigen‐specific cytokine responses of mucosal lymphocytes, obtained from a site of HPV infection, have been demonstrated. This finding clearly illustrates the use of intracellular cytokine staining for investigation of low precursor frequency single‐cell antigen‐specific responses in lymphocytes harvested from mucosal sites with HPV infection. J. Med. Virol. 67:234–240, 2002. © 2002 Wiley‐Liss, Inc.


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