Association between Chronic Environmental Lead (Pb) Exposure and Cytokines in Males and Females of Reproductive Age from Kabwe, Zambia

Int J Environ Res Public Health. 2023 Apr 20;20(8):5596. doi: 10.3390/ijerph20085596.

Abstract

Lead (Pb) poisoning remains a great public health challenge globally known to induce a wide range of ailments in both children and adults. The current study investigated the association of chronic environmental Pb exposure and immunomodulatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin-8 (IL-8) in adult males and females living in Kabwe, Zambia. The standard human cytokine/chemokine Milliplex assay was used to quantify plasma cytokines from four groups categorized as low (<10 μg/dL) and high (>10 μg/dL) blood lead level (BLL) groups, namely, low BLL female (n = 47; BLL = 3.76 μg/dL), low BLL Male (n = 43; BLL = 4.13 μg/dL), high BLL female (n = 21; BLL = 23.5 μg/dL), and high BLL male (n = 18; BLL = 23.7 μg/dL), respectively. The low BLL group was associated with increased TNF-α levels, and the high BLL group was associated with reduced TNF-α levels in female subjects. No associations between BLL and the levels of IL-8 and TNF-α cytokines were observed in either females or males, respectively. A negative correlation between BLL and TNF-α was found in female subjects, suggesting that an increase in BLL accompanied by a reduction in TNF-α. The reduced levels of circulating TNF-α in female subjects suggest that chronic Pb exposure could predispose females to immune and inflammation-related disorders than their male counterparts. Further studies are recommended to ascertain the impact of chronic Pb exposure on immunomodulatory cytokines, especially in females.

Keywords: chronic; cytokines; immunomodulatory; lead; sex-linked.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Cytokines
  • Environmental Exposure / adverse effects
  • Environmental Exposure / analysis
  • Female
  • Humans
  • Interleukin-8
  • Lead Poisoning*
  • Lead* / toxicity
  • Male
  • Tumor Necrosis Factor-alpha
  • Zambia / epidemiology

Substances

  • Lead
  • Interleukin-8
  • Cytokines
  • Tumor Necrosis Factor-alpha

Grants and funding

This work was financially supported by the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan; 18KK0287 (MI), 21H04919 (MI), 20K20633 (SMMN) and 23H03545 (SMMN). The authors would like to acknowledge the JST/JICA SATREPS (Science and Technology Research Partnership for Sustainable Development; No. JPMJSA1501) and aXis (Accelerating Social Implementation for SDGs Achievement; No. JPMJAS2001) funded by JST for the financial support. This study was also supported by JST AJ-CORE Project (MI), JSPS CORE to CORE program (MI, SMMN), Hokkaido University SOUSEI-TOKUTEI Specific Research Projects (MI), JSPS Bilateral Open Partnership Joint Research Projects (JPJSBP120209902; SMMN), and the Japan Prize Foundation (SMMN).