Macrophage and CD8 T cell discordance are associated with acute lung allograft dysfunction progression
Evidence level: prospective single-cell RNA sequencing cohort; abstract-only
Lavage cell sequencing in 45 recipients found a macrophage cluster and a CD8 T cell cluster that distinguished ALAD with later decline from ALAD that recovered or stable function.
As of . Primary source: Publisher record via DOI.
Summary
Acute lung allograft dysfunction (ALAD) is an imprecise syndrome that raises concern for the onset of CLAD. The study collected bronchoalveolar lavage prospectively for single-cell RNA sequencing from 17 ALAD cases with subsequent decline, 13 ALAD cases that resolved and 15 recipients with stable lung function. A CD8 T cell cluster resembling tissue-resident memory cells and a macrophage cluster with an anti-inflammatory signature best identified the ALAD cases with decline. The abstract reports that these macrophages signalled to activated CD8 T cells through several pathways. The authors suggest that anti-inflammatory lavage macrophages may protect against CLAD by suppressing CD8 T cells, and state that these populations merit further assessment in additional cohorts. The suggestion is a hypothesis, not a demonstrated mechanism.
Details
- doi
- 10.1016/j.healun.2024.02.007
- pmid
- 38367738
- authors
- Calabrese DR, Ekstrand CA, Yellamilli S, Singer JP, Hays SR, Leard LE, Shah RJ, Venado A, Kolaitis NA, Perez A, Combes A, Greenland JR
- journal
- The Journal of Heart and Lung Transplantation
- year
- 2024
- volume
- 43
- issue
- 7
- pages
- 1074-1086
Sources and links
- Publisher record via DOI (primary)
- PubMed 38367738
Related
Links from this record
- supports: Acute lung allograft dysfunction (ALAD)
- related to: Innate immune activation
- related to: Cytotoxic and senescent T cells
- related to: Airway transcriptomic signatures
Linked from (derived)
Known gaps in this record
- full text not read (abstract only)
- funding statement and grant numbers
- author affiliations
- centre or centres not stated in the abstract
Information resource only. Not medical advice. Not a substitute for the care of the patient's transplant team.