Escalation of Germinal Center Responses in Chronic Litomosoides sigmodontis Filarial Infection

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Teresa Steffen, Jesuthas Ajendra, Marianne Koschel, Alexander Palmen, Hannah Wegner, Frederic Risch, Luisa Bach, Manuel Ritter, Marc P. Hübner, Dirk Baumjohann
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Abstract

T follicular helper (TFH) cells are the primary CD4+ T helper cell subset providing help to B cells for efficient antibody responses in vaccination, allergy, autoimmunity, and infectious diseases. Despite their critical involvement in immunity, TFH cells’ specific role in filarial infections remains unclear. Using the rodent filarial model Litomosoides sigmodontis, we examined TFH and germinal center (GC) B cell responses in lung-draining mediastinal lymph nodes (medLNs) over a 110-day infection period in naive and infected wildtype (WT) BALB/c mice, as well as eosinophil-deficient dblGATA mice, using flow cytometry and ELISA. We observed robust and prolonged TFH and GC B cell responses in medLNs of infected BALB/c mice, along with enduring IgG1 antibody responses next to a persistent systemic humoral immune response. We further provide evidence of dysregulated TFH/T follicular regulatory (TFR) cell ratios in medLNs. Finally, elevated TFH cell frequencies in medLNs of dblGATA mice reaffirm the significant role of eosinophils during chronic infection. In conclusion, our findings provide novel insights into population changes of TFH and GC B cells during filarial infection.

慢性鹅口疮丝虫病感染中生发中心反应的升级
T滤泡辅助细胞(TFH)是主要的CD4+ T辅助细胞亚群,在疫苗接种、过敏、自身免疫和感染性疾病中帮助B细胞进行有效的抗体反应。尽管TFH细胞在免疫中起关键作用,但其在丝虫病感染中的具体作用仍不清楚。使用啮齿动物丝虫模型sigmodontis,我们使用流式细胞术和ELISA检测了在110天的感染期内,未感染和感染野生型(WT) BALB/c小鼠以及嗜酸性粒细胞缺乏的dblGATA小鼠肺排纵隔淋巴结(medLNs)中TFH和生发中心(GC) B细胞的反应。我们在感染BALB/c小鼠的medLNs中观察到强大且持久的TFH和GC B细胞反应,以及持久的IgG1抗体反应和持续的全身体液免疫反应。我们进一步提供了在medLNs中TFH/T滤泡调节(TFR)细胞比例失调的证据。最后,dblGATA小鼠medLNs中TFH细胞频率的升高再次证实了嗜酸性粒细胞在慢性感染中的重要作用。总之,我们的研究结果为丝虫病感染期间TFH和GC B细胞的种群变化提供了新的见解。
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来源期刊
CiteScore
8.30
自引率
3.70%
发文量
224
审稿时长
2 months
期刊介绍: The European Journal of Immunology (EJI) is an official journal of EFIS. Established in 1971, EJI continues to serve the needs of the global immunology community covering basic, translational and clinical research, ranging from adaptive and innate immunity through to vaccines and immunotherapy, cancer, autoimmunity, allergy and more. Mechanistic insights and thought-provoking immunological findings are of interest, as are studies using the latest omics technologies. We offer fast track review for competitive situations, including recently scooped papers, format free submission, transparent and fair peer review and more as detailed in our policies.
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