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. 2014 Aug 15;15(8):14269–14297. doi: 10.3390/ijms150814269

Table 4.

Evidence and hypothesized mechanisms underlying autoimmune disease associations with smoking, silica, and solvents.

Exposure-Disease Association in Humans Evidence on in Vitro and in Vivo Mechanisms
Smoking and seropositive-RA Post-translational modification—antigen citrullination and anti-cyclic citrullinated peptides (CCP) antibodies [80,82];
Nicotine and Th17 activation [86,87];
Upregulation of heat shock gene expression [84] *;
Disease relevant autoantibodies (RF, anti-HSP70) [85] *.
Silica and RA/SLE/SSc/ANCA-vasculitis Aggravation of lupus in animal models [88];
Adjuvant effect-apoptotic debris [88];
Dysregulation of apoptosis [90] *;
Disease relevant autoantibodies (anti-dsDNA, anti-Ro/SSA, anti-La/SSB antibodies in silica associated SLE) [91] *;
Altered CD4+/CD4+ CD25+ T cell ratio [89] *.
Solvents and SSc Accelerated autoimmunity in animal models [93]
SSc disease relevant autoantibodies (anti-Scl-70) [92]
Increased IFN-γ, reduced IL-4 [93] *

* Similar observations made in animal studies.