Immune Modulation by Cadmium and Lead in the Acute Reporter Antigen–Popliteal Lymph Node Assay

• Published in: Toxicological sciences Vol. 91; no. 1; pp. 113 - 122
• Main Authors: Carey, John B., Allshire, Ashley, van Pelt, Frank N.
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01-05-2006
• Subjects: Animals; B-Lymphocytes - drug effects; B-Lymphocytes - immunology; cadmium; Cadmium - toxicity; Flow Cytometry; heavy metals; Immunity, Cellular - drug effects; immunotoxicity; lead; Lead - toxicity; Lymph Nodes - cytology; Lymph Nodes - drug effects; Lymph Nodes - immunology; Lymphocyte Subsets; mercury; Mice; Mice, Inbred BALB C; popliteal lymph node assay; T-Lymphocytes - drug effects; T-Lymphocytes - immunology
• ISSN: 1096-6080; 1096-0929
• DOI: 10.1093/toxsci/kfj142

Immune modulation by heavy metals may cause serious adverse health effects in humans, although the mechanisms involved are not well understood. Both cadmium and lead are important environmental and occupational toxins. Therefore, in the current study, the costimulatory/adjuvant effects and the T-cell–activating potential of these metals (i.e., CdCl2 and PbCl2), are examined. These immune-modulating properties are critical in the development of conditions such as allergy, hypersensitivity, and autoimmunity. Using the direct popliteal lymph node assay (PLNA) and reporter antigen–popliteal lymph node assay (RA-PLNA) both metals were examined individually for immunotoxicity. Mercury (i.e., HgCl2) was included for comparative purposes as its effects in the RA-PLNA are well documented. Seven days following a single footpad injection containing metal and/or RA (trinitrophenyl-ovalbumin [TNP-OVA] or TNP-Ficoll), BALB/c mice were sacrificed and the popliteal lymph nodes (PLNs) removed. PLN cellularity, TNP-specific antibody-secreting cells (ASCs), and lymphocyte subsets were assessed. All three metals strongly stimulated T- and B-cell proliferation and ASC production following coinjection with the RA TNP-OVA. In each case, ASC production was skewed towards the IgG1 isotype. In addition, all three metals induced IgG production to TNP-Ficoll (although relatively weakly in the case of Cd). These results show that each of these metals can provide adjuvant signals to promote lymphocyte proliferation and enhance adaptive immune responses to unrelated antigens. Skewing of immune responses towards T helper type 2 responses suggests that each of these metals can enhance allergic and hypersensitivity reactions to environmental antigens. Furthermore, the induction of IgG responses to TNP-Ficoll, a T-cell–independent antigen, indicates that each of these metals can activate neoantigen-specific T cells. T-cell activation by metals can lead to metal hypersensitivity and has been implicated in the development of autoimmunity. This is the first report of immune modulation by CdCl2 and PbCl2 in the RA-PLNA.