T cell infiltration into the brain triggers pulmonary dysfunction in murine Cryptococcus-associated IRIS.
Tasuku KawanoJinyan ZhouShehata AnwarHaneen SalahAndrea H DayalYuzuki IshikawaKatelyn BoetelTomoko TakahashiKamal SharmaMakoto InouePublished in: Nature communications (2023)
Cryptococcus-associated immune reconstitution inflammatory syndrome (C-IRIS) is a condition frequently occurring in immunocompromised patients receiving antiretroviral therapy. C-IRIS patients exhibit many critical symptoms, including pulmonary distress, potentially complicating the progression and recovery from this condition. Here, utilizing our previously established mouse model of unmasking C-IRIS (CnH99 preinfection and adoptive transfer of CD4 + T cells), we demonstrated that pulmonary dysfunction associated with the C-IRIS condition in mice could be attributed to the infiltration of CD4 + T cells into the brain via the CCL8-CCR5 axis, which triggers the nucleus tractus solitarius (NTS) neuronal damage and neuronal disconnection via upregulated ephrin B3 and semaphorin 6B in CD4 + T cells. Our findings provide unique insight into the mechanism behind pulmonary dysfunction in C-IRIS and nominate potential therapeutic targets for treatment.
Keyphrases
- pulmonary hypertension
- oxidative stress
- mouse model
- antiretroviral therapy
- cerebral ischemia
- ejection fraction
- end stage renal disease
- white matter
- newly diagnosed
- hiv infected
- resting state
- human immunodeficiency virus
- cell therapy
- prognostic factors
- dendritic cells
- regulatory t cells
- high fat diet induced
- type diabetes
- case report
- immune response
- insulin resistance
- hepatitis c virus
- sleep quality
- hiv infected patients
- combination therapy
- liver injury
- patient reported outcomes
- depressive symptoms
- acute respiratory distress syndrome
- patient reported
- electron transfer
- mechanical ventilation