Systemic toxoplasma infection triggers a long-term defect in the generation and function of naive T lymphocytes

J Exp Med. 2016 Nov 14. pii: jem.20151636. [Epub ahead of print]

Kugler DG¹, Flomerfelt FA², Costa DL¹, Laky K³, Kamenyeva O⁴, Mittelstadt PR⁵, Gress RE², Rosshart SP⁶, Rehermann B⁶, Ashwell JD⁵, Sher A⁷, Jankovic D⁷.

Because antigen-stimulated naive T cells either die as effectors or enter the activated/memory pool, continuous egress of new T lymphocytes from thymus is essential for maintenance of peripheral immune homeostasis. Unexpectedly, we found that systemic infection with the protozoan Toxoplasma gondii triggers not only a transient increase in activated CD4⁺ Th1 cells but also a persistent decrease in the size of the naive CD4⁺ T lymphocyte pool. This immune defect is associated with decreased thymic output and parasite-induced destruction of the thymic epithelium, as well as disruption of the overall architecture of that primary lymphoid organ. Importantly, the resulting quantitative and qualitative deficiency in naive CD4⁺ T cells leads to an immunocompromised state that both promotes chronic toxoplasma infection and leads to decreased resistance to challenge with an unrelated pathogen. These findings reveal that systemic infectious agents, such as T. gondii, can induce long-term immune alterations associated with impaired thymic function. When accumulated during the lifetime of the host, such events, even when occurring at low magnitude, could be a contributing factor in immunological senescence.

PMID:

27849554

DOI:

10.1084/jem.20151636

[PubMed - as supplied by publisher]