Causal association between the peripheral immunity and the risk and disease severity of multiple sclerosis
Каузальная связь между периферическим иммунитетом и риском и тяжестью течения рассеянного склероза
2024-02-08
SCID: 54.1/agwf6f3v
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CD4+ T cellsIL-2RaMendelian randomizationmultiple sclerosis riskperipheral immune cell counts
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Abstract (AI)
Background Growing evidence links immunological responses to Multiple sclerosis (MS), but specific immune factors are still unclear. Methods Mendelian randomization (MR) was performed to investigate the association between peripheral hematological traits, MS risk, and its severity. Then, further subgroup analysis of immune counts and circulating cytokines and growth factors were performed. Results MR revealed higher white blood cell count (OR [95%CI] = 1.26 [1.10,1.44], P = 1.12E-03, P adjust = 3.35E-03) and lymphocyte count (OR [95%CI] = 1.31 [1.15,1.50], P = 5.37E-05, P adjust = 3.22E-04) increased the risk of MS. In further analysis, higher T cell absolute count (OR [95%CI] = 2.04 [1.36,3.08], P = 6.37E-04, P adjust = 2.19E-02) and CD4 + T cell absolute count (OR [95%CI] = 2.11 [1.37,3.24], P = 6.37E-04, P adjust = 2.19E-02), could increase MS risk. While increasing CD25 ++ CD4 + T cell absolute count (OR [95%CI] = 0.75 [0.66,0.86], P = 2.12E-05, P adjust = 1.72E-03), CD25 ++ CD4 + T cell in T cell (OR [95%CI] = 0.79[0.70,0.89], P = 8.54E-05, P adjust = 5.29E-03), CD25 ++ CD4 + T cell in CD4 + T cell (OR [95%CI] = 0.80[0.72,0.89], P = 1.85E-05, P adjust = 1.72E-03), and CD25 ++ CD8 + T cell in T cell (OR [95%CI] = 0.68[0.57,0.81], P = 2.22E-05, P adjust = 1.72E-03), were proved to be causally defensive for MS. For the disease severity, the suggestive association between some traits related to CD4 + T cell, Tregs and MS severity were demonstrated. Moreover, elevated levels of IL-2Ra had a detrimental effect on the risk of MS (OR [95%CI] = 1.22 [1.12,1.32], P = 3.20E-06, P adjust = 1.34E-04). Conclusions This study demonstrated a genetically predicted causal relationship between elevated peripheral immune cell counts and MS. Subgroup analysis revealed a specific contribution of peripheral immune cells, holding potential for further investigations into the underlying mechanisms of MS and its severity.
Key Findings
1
Elevated genetically predicted circulating IL-2Ra levels increase MS risk (OR=1.22, 95% CI 1.12–1.32, P=3.20E-06, P adjust=1.34E-04); some CD4+ T cell and Treg–related traits show suggestive associations with MS severity.
2
Genetically higher lymphocyte count causally increases risk of multiple sclerosis (OR=1.31, 95% CI 1.15–1.50, P=5.37E-05, P adjust=3.22E-04).
3
Genetically higher total white blood cell count causally increases risk of multiple sclerosis (OR=1.26, 95% CI 1.10–1.44, P=1.12E-03, P adjust=3.35E-03).
4
Higher genetically predicted T cell and CD4+ T cell absolute counts strongly increase MS risk (T cells OR=2.04, CD4+ OR=2.11; both P=6.37E-04, P adjust=2.19E-02).
5
Higher genetically predicted regulatory T cell–related subsets (CD25++ CD4+ absolute count and proportions, and CD25++ CD8+ in T cells) are causally protective against MS (ORs 0.68–0.80, all adjusted P ≤ 5.29E-03).
Research Object
Peripheral immune system / peripheral hematological and immune cell traits (peripheral immune cell counts, circulating cytokines and growth factors)
Research Subject
Causal associations between peripheral immune traits (cell counts and soluble factors) and multiple sclerosis risk and disease severity
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2024-02-08
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