PMID- 36808577 OWN - NLM STAT- MEDLINE DCOM- 20231023 LR - 20231023 IS - 1591-9528 (Electronic) IS - 1591-8890 (Linking) VI - 23 IP - 6 DP - 2023 Oct TI - T lymphocyte subsets and immunoglobulin and complement levels are associated with the infection status of patients with antineutrophil cytoplasmic antibody-associated vasculitis. PG - 2877-2884 LID - 10.1007/s10238-023-01021-4 [doi] AB - BACKGROUND: Infection is the leading cause of death in patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV). The aim of this study was to characterize the immunological features of infectious events occurring in patients with newly diagnosed AAV and to identify possible risk factors associated with infection. METHODS: The T lymphocyte subsets, immunoglobulin, and complement levels of the groups were compared between infected group and the noninfected group. Further, regression analysis was conducted to determine the association of each variable with the risk of infection. RESULTS: 280 patients with newly diagnosed AAV were enrolled. The average levels of CD3(+) T cells (720.0 vs. 920.5, P < 0.001), CD3(+)CD4(+) T cells (392.0 vs. 547.0, P < 0.001), and CD3(+)CD8(+) T cells (248.0 vs. 335.0, P = 0.001), serum IgG (11.66 g/L vs. 13.59 g/L, P = 0.002), IgA (1.70 g/L vs. 2.44 g/L, P < 0.001), C3 (1.03 g/L vs. 1.09 g/L, P = 0.015), and C4 (0.24 g/L vs. 0.27 g/L, P < 0.001) were significantly lower in the infected group than in the noninfected group. The levels of CD3(+)CD4(+) T cells (adjusted OR 0.997, P = 0.018), IgG (adjusted OR 0.804, P = 0.004), and C4 (adjusted OR 0.001, P = 0.013) were found independently associated with infection. CONCLUSIONS: Patients of infected AAV and those without infection differ in T lymphocyte subsets and immunoglobulin and complement levels. Furthermore, CD3(+)CD4(+) T cells counts and serum IgG and C4 levels were independent risk factors with infection in patients with newly diagnosed AAV. CI - (c) 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG. FAU - Liu, Rui AU - Liu R AD - Department of Rheumatology and Immunology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. FAU - Li, Mengdi AU - Li M AD - Department of Rheumatology and Immunology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. FAU - Zhang, Lei AU - Zhang L AD - Department of Rheumatology and Immunology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. FAU - Wang, Yan AU - Wang Y AD - Department of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. FAU - Li, Wei AU - Li W AUID- ORCID: 0000-0002-4073-4397 AD - Department of Rheumatology and Immunology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. libuwei2011@163.com. FAU - Liu, Shengyun AU - Liu S AUID- ORCID: 0000-0002-0426-1705 AD - Department of Rheumatology and Immunology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. fccliusy2@zzu.edu.cn. LA - eng PT - Journal Article DEP - 20230219 PL - Italy TA - Clin Exp Med JT - Clinical and experimental medicine JID - 100973405 RN - 0 (Antibodies, Antineutrophil Cytoplasmic) RN - 0 (Immunoglobulin G) SB - IM MH - Humans MH - *Antibodies, Antineutrophil Cytoplasmic MH - CD8-Positive T-Lymphocytes MH - T-Lymphocyte Subsets MH - *Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis MH - Immunoglobulin G OTO - NOTNLM OT - ANCA-associated vasculitis OT - Complement OT - Immunoglobulin OT - Infection OT - T lymphocyte subset EDAT- 2023/02/23 06:00 MHDA- 2023/10/23 12:41 CRDT- 2023/02/22 12:56 PHST- 2023/01/22 00:00 [received] PHST- 2023/02/05 00:00 [accepted] PHST- 2023/10/23 12:41 [medline] PHST- 2023/02/23 06:00 [pubmed] PHST- 2023/02/22 12:56 [entrez] AID - 10.1007/s10238-023-01021-4 [pii] AID - 10.1007/s10238-023-01021-4 [doi] PST - ppublish SO - Clin Exp Med. 2023 Oct;23(6):2877-2884. doi: 10.1007/s10238-023-01021-4. Epub 2023 Feb 19.