Malaria-specific Type 1 regulatory T cells are more abundant in first pregnancies and associated with placental malaria

被引：4

作者：

Kirosingh, Adam S. ^{[1
]}

Delmastro, Alea ^{[1
]}

Kakuru, Abel ^{[2
]}

van der Ploeg, Kattria ^{[1
]}

Bhattacharya, Sanchita ^{[3
]}

Press, Kathleen D. ^{[1
]}

Ty, Maureen ^{[1
]}

de la Parte, Lauren ^{[1
]}

Kizza, Jimmy ^{[4
]}

Muhindo, Mary ^{[4
]}

Devachanne, Sebastien ^{[5
]}

Gamain, Benoit ^{[5
]}

Nankya, Felistas ^{[2
]}

Musinguzi, Kenneth ^{[2
]}

Rosenthal, Philip J. ^{[3
]}

Feeney, Margaret E. ^{[3
]}

Kamya, Moses ^{[2
,4
]}

Dorsey, Grant ^{[3
]}

Jagannathan, Prasanna ^{[1
,6
]}

机构：

[1] Stanford Univ, Sch Med, Stanford, CA USA

[2] Infect Dis Res Collaborat, Kampala, Uganda

[3] Univ Calif San Francisco, San Francisco, CA USA

[4] Makerere Univ, Kampala, Uganda

[5] Univ Paris Cite, INSERM, BIGR, F-75014 Paris, France

[6] Stanford Univ, Dept Med, Div Infect Dis & Geog Med, 300 Pasteur Dr, Stanford, CA 94305 USA

来源：

EBIOMEDICINE | 2023年 / 95卷

关键词：

Malaria; Pregnancy; Gravidity; CD4(+) T cells; Placental malaria; Immunity; PLASMODIUM-FALCIPARUM; IL-10; PRODUCTION; SULFADOXINE-PYRIMETHAMINE; CHONDROITIN SULFATE; DIFFERENTIATION; PROTECTION; RESPONSES; CYTOKINES; MEMORY; WOMEN;

D O I：

10.1016/j.ebiom.2023.104772

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Background Malaria in pregnancy (MIP) causes higher morbidity in primigravid compared to multigravid women; however, the correlates and mechanisms underlying this gravidity-dependent protection remain incompletely understood. We aimed to compare the cellular immune response between primigravid and multigravid women living in a malaria-endemic region and assess for correlates of protection against MIP. Methods We characterised the second trimester cellular immune response among 203 primigravid and multigravid pregnant women enrolled in two clinical trials of chemoprevention in eastern Uganda, utilizing RNA sequencing, flow cytometry, and functional assays. We compared responses across gravidity and determined associations with parasitaemia during pregnancy and placental malaria. Findings Using whole blood RNA sequencing, no significant differentially expressed genes were identified between primigravid (n = 12) and multigravid (n = 11) women overall (log 2(FC) > 2, FDR < 0.1). However, primigravid (n = 49) women had higher percentages of malaria-specific, non-naive CD4(+) T cells that co-expressed IL-10 and IFN gamma compared with multigravid (n = 85) women (p = 0.000023), and higher percentages of these CD4(+) T cells were associated with greater risks of parasitaemia in pregnancy (Rs = 0.49, p = 0.001) and placental malaria (p = 0.0073). These IL-10 and IFN. co-producing CD4(+) T cells had a genomic signature of Tr1 cells, including expression of transcription factors cMAF and BATF and cell surface makers CTLA4 and LAG-3. Interpretation Malaria-specific Tr1 cells were highly prevalent in primigravid Ugandan women, and their presence correlated with a higher risk of malaria in pregnancy. Understanding whether suppression of Tr1 cells plays a role in naturally acquired gravidity-dependent immunity may aid the development of new vaccines or treatments for MIP. Copyright (c) 2023 The Author(s). Published by Elsevier B.V.

引用

页数：19

共 90 条

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