Tissue expression of TGF-β1 in uterine cervical samples from HIV/AIDS patients

被引:3
作者
Carneiro, Thiago X. [2 ]
Pacheco, Juliana T. [2 ]
Xavier, Marilia B. [1 ,2 ]
Quaresma, Juarez A. S. [1 ,2 ]
机构
[1] Fed Univ Para, Nucleo Med Trop, BR-66059 Belem, Para, Brazil
[2] Univ Estado Para, Ctr Ciencias Biol & Saude, Belem, Para, Brazil
关键词
Transforming growth factor-beta; Cervical intraepithelial neoplasia; Cervical Neoplasms; Human immunodeficiency virus; Acquired immunodeficiency syndrome; HUMAN-IMMUNODEFICIENCY-VIRUS; GROWTH-FACTOR-BETA; CARCINOMA CELL-LINES; TGF-BETA; INTRAEPITHELIAL NEOPLASIA; HIV-INFECTION; TRANSFORMING GROWTH-FACTOR-BETA-1; DIFFERENTIAL RESPONSE; WOMEN; CANCER;
D O I
10.1016/j.micpath.2012.03.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Case-control study based on the immunohistochemistry for TGF-beta 1 evaluation of cervical samples obtained from two groups of women: CIN/HIV- and CIN/HIV+. Eleven women infected with HIV and with a histopathological diagnosis of CIN were included. The control group consisted of 12 patients with CIN. Cervical tissue samples obtained from all patients were submitted to histopathology and semiquantitative analysis of immunostaining for TGF-beta 1 protein. In addition, the peripheral CD4+ cell count and viral load were evaluated in HIV + patients. Tissue expression of the cytokine was higher in the CIN/HIV+ group compared to control (p = 0.0023). In addition, higher TGF-beta 1 expression was observed in higher grade cervical lesions in the two groups. There was a trend toward a direct correlation between peripheral CD4+ T cell count and tissue TGF-beta 1, and toward an inverse correlation between viral load and cytokine expression. Thus, TGF-beta 1 was more marked in situations in which cervical lesions are known to present a more aggressive behavior, suggesting that this cytokine is involved in the pathogenesis of tumor growth in these lesions. Tissue expression of TGF-beta 1 is increased in cervical samples from HIV-infected women with CIN. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:44 / 48
页数:5
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