Adults from Kisumu, Kenya have robust γδ T cell responses to Schistosoma mansoni, which are modulated by tuberculosis

• Published in: PLoS neglected tropical diseases Vol. 14; no. 10; p. e0008764
• Main Authors: McLaughlin, Taryn A, Khayumbi, Jeremiah, Ongalo, Joshua, Matete, Daniel, Tonui, Joan, Muchiri, Benson, Sasser, Loren E, Campbell, Angela, Allana, Salim, Ouma, Samuel Gurrion, Hayara, Felix Odhiambo, Gandhi, Neel R, Day, Cheryl L
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.10.2020; Public Library of Science (PLoS)
• Subjects: Adult; Adults; Animals; Antibodies; Antibodies, Helminth; Antigens; Biology and Life Sciences; Cell proliferation; Cells; Cohorts; Coinfection - immunology; Coinfection - microbiology; Coinfection - parasitology; Cytokines; Defence mechanisms; Disease; Eggs; Epidemiology; Female; Flow cytometry; HIV; Human immunodeficiency virus; Humans; Immune response; Immune system; Immunity; Infections; Interferon; Interferon-gamma - immunology; Interleukin 4; Interleukin-4 - immunology; Kenya; Life cycle; Life cycles; Lymphocytes; Lymphocytes T; Male; Medical research; Medicine and Health Sciences; Microscopy; Middle Aged; Morbidity; Mycobacterium tuberculosis - genetics; Mycobacterium tuberculosis - immunology; Mycobacterium tuberculosis - physiology; Pathogens; Proliferation; Public health; Research and Analysis Methods; Schistosoma mansoni; Schistosoma mansoni - genetics; Schistosoma mansoni - immunology; Schistosoma mansoni - physiology; Schistosomiasis mansoni - immunology; Schistosomiasis mansoni - parasitology; Supervision; T-Lymphocytes - immunology; Tropical diseases; Tuberculosis; Tuberculosis - immunology; Tuberculosis - microbiology; Tumor necrosis factor-α; Vaccines; Worms; γ-Interferon; Kenya; Atlanta Georgia; Georgia; United States > US; Sub-Saharan Africa
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0008764

Schistosoma mansoni (SM) is a parasitic helminth that infects over 200 million people and causes severe morbidity. It undergoes a multi-stage life cycle in human hosts and as such stimulates a stage-specific immune response. The human T cell response to SM is complex and varies throughout the life cycle of SM. Relative to the wealth of information regarding the immune response to SM eggs, little is known about the immune response to the adult worm. In addition, while a great deal of research has uncovered mechanisms by which co-infection with helminths modulates immunity to other pathogens, there is a paucity of data on the effect of pathogens on immunity to helminths. As such, we sought to characterize the breadth of the T cell response to SM and determine whether co-infection with Mycobacterium tuberculosis (Mtb) modifies SM-specific T cell responses in a cohort of HIV-uninfected adults in Kisumu, Kenya. SM-infected individuals were categorized into three groups by Mtb infection status: active TB (TB), Interferon-γ Release Assay positive (IGRA+), and Interferon-γ Release Assay negative (IGRA-). U.S. adults that were seronegative for SM antibodies served as naïve controls. We utilized flow cytometry to characterize the T cell repertoire to SM egg and worm antigens. We found that T cells had significantly higher proliferation and cytokine production in response to worm antigen than to egg antigen. The T cell response to SM was dominated by γδ T cells that produced TNFα and IFNγ. Furthermore, we found that in individuals infected with Mtb, γδ T cells proliferated less in response to SM worm antigens and had higher IL-4 production compared to naïve controls. Together these data demonstrate that γδ T cells respond robustly to SM worm antigens and that Mtb infection modifies the γδ T cell response to SM.