Arsenic exposure associated T cell proliferation, smoking, and vitamin D in Bangladeshi men and women

被引:9
作者
Burchiel, Scott W. [1 ]
Lauer, Fredine T. [1 ]
Factor-Litvak, Pam [2 ]
Liu, Xinhua [3 ]
Islam, Tariqul [4 ]
Eunus, Mahbubul [4 ]
Abu Horayara, M. [4 ]
Islam, Md. Tariqul [4 ]
Rahman, Mizanour [4 ]
Ahmed, Alauddin [4 ]
Cremers, Serge [5 ]
Nandakumar, Renu [6 ]
Ahsan, Habibul [7 ]
Olopade, Christopher [8 ]
Graziano, Joseph [9 ]
Parvez, Faruque [9 ]
机构
[1] Univ New Mexico, Coll Pharm, Dept Pharmaceut Sci, Albuquerque, NM 87131 USA
[2] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
[3] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY USA
[4] Univ Chicago & Columbia Univ Field Res Off, Dhaka, Bangladesh
[5] Columbia Univ, Dept Pathol & Cell Biol, Med Ctr, New York, NY USA
[6] Columbia Univ, Irving Inst Clin & Translat Res, Med Ctr, New York, NY USA
[7] Univ Chicago, Dept Hlth Studies, Chicago, IL 60637 USA
[8] Univ Chicago, Med Ctr, Chicago, IL 60637 USA
[9] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
来源
PLOS ONE | 2020年 / 15卷 / 06期
关键词
ENVIRONMENTALLY RELEVANT CONCENTRATIONS; CYTOKINE SECRETION; CHILDREN; THYMUS; INHIBITION; DEFICIENCY; ACTIVATION;
D O I
10.1371/journal.pone.0234965
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There are limited data examining the consequences of environmental exposure to arsenic on the immune system in adults, particularly among smokers. Smoking has been shown to exacerbate or contribute to impaired immune function in men chronically exposed to arsenic. In contrast, vitamin D (VitD) is known to have a positive influence on innate and adaptive immune responses. The effect of circulating VitD on arsenic-associated immune dysfunction is not known. Here we examine the relationship of arsenic exposure and T cell proliferation (TCP), a measure of immune responsiveness, and circulating VitD among adult men and women in Bangladesh. Arsenic exposure was assessed using total urinary arsenic as well as urinary arsenic metabolites all adjusted for urinary creatinine. TCP was measuredex vivoin cryopreserved peripheral blood mononuclear cells from 614 adult participants enrolled in the Bangladesh Health Effects of Arsenic Longitudinal Study; serum VitD was also evaluated. The influence of cigarette smoking on arsenic-induced TCP modulation was assessed only in males as there was an inadequate number of female smokers. These studies show that arsenic suppressed TCP in males. The association was significantly strong in male smokers and to a lesser extent in male non-smokers. Interestingly, we found a strong protective effect of high/sufficient serum VitD levels on TCP among non-smoking males. Furthermore, among male smokers with low serum VitD ( square cup 20 ng/ml), we found a strong suppression of TCP by arsenic. On the other hand, high VitD (>20 ng/ml) was found to attenuate effects of arsenic on TCP among male-smokers. Overall, we found a strong protective effect of VitD, when serum levels were >20 ng/ml, on arsenic-induced inhibition of TCP in men, irrespective of smoking status. To our knowledge this is the first large study of immune function in healthy adult males and females with a history of chronic arsenic exposure.
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页数:13
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