Dynamic MAIT Cell Recovery after Severe COVID-19 Is Transient with Signs of Heterogeneous Functional Anomalies.
Tobias KammannJean-Baptiste GorinTiphaine ParrotYu GaoAndrea PonzettaJohanna EmgårdKimia T MalekiTakuya SekineOlga Rivera-Ballesterosnull nullSara Gredmark-RussOlav RooyackersMagdalena SkagerbergLars I ErikssonAnna Norrby-TeglundJeffrey Y W MakDavid P FairlieNiklas K BjörkströmJonas KlingströmHans-Gustaf LjunggrenSoo AlemanMarcus BuggertKristoffer StrålinJohan K SandbergPublished in: Journal of immunology (Baltimore, Md. : 1950) (2024)
Mucosal-associated invariant T (MAIT) cells are an abundant population of unconventional T cells in humans and play important roles in immune defense against microbial infections. Severe COVID-19 is associated with strong activation of MAIT cells and loss of these cells from circulation. In the present study, we investigated the capacity of MAIT cells to recover after severe COVID-19. In longitudinal paired analysis, MAIT cells initially rebounded numerically and phenotypically in most patients at 4 mo postrelease from the hospital. However, the rebounding MAIT cells displayed signs of persistent activation with elevated expression of CD69, CD38, and HLA-DR. Although MAIT cell function was restored in many patients, a subgroup displayed a predominantly PD-1high functionally impaired MAIT cell pool. This profile was associated with poor expression of IFN-γ and granzyme B in response to IL-12 + L-18 and low levels of polyfunctionality. Unexpectedly, although the overall T cell counts recovered, normalization of the MAIT cell pool failed at 9-mo follow-up, with a clear decline in MAIT cell numbers and a further increase in PD-1 levels. Together, these results indicate an initial transient period of inconsistent recovery of MAIT cells that is not sustained and eventually fails. Persisting MAIT cell impairment in previously hospitalized patients with COVID-19 may have consequences for antimicrobial immunity and inflammation and could potentially contribute to post-COVID-19 health problems.
Keyphrases
- induced apoptosis
- cell cycle arrest
- coronavirus disease
- sars cov
- single cell
- healthcare
- stem cells
- poor prognosis
- signaling pathway
- cell therapy
- cell death
- early onset
- mental health
- randomized controlled trial
- emergency department
- endoplasmic reticulum stress
- newly diagnosed
- patient reported outcomes
- study protocol
- pi k akt
- prognostic factors
- ulcerative colitis
- african american