Single-cell RNA sequencing (scRNA-seq) allows cell classification using genome-wide transcriptional state; however, high-dimensional transcriptomic profiles, and the unsupervised analyses employed to interpret them, provide a systematically different view of biology than well-established functional/lineage definitions of immunocytes. Understanding these differences and limits is essential for accurate interpretation of these rich data. We present the Rhesus Immune Reference Atlas (RIRA), the first immune-focused macaque single-cell multi-tissue atlas. We contrasted transcriptional profiles against immune lineages, using surface protein and marker genes as ground truth. While the pattern of clustering can align with cell type, this is not always true. Especially within T and natural killer (NK) cells, many functionally distinct subsets lack defining markers, and strong shared expression programs, such as cytotoxicity, result in systematic intermingling by unsupervised clustering. We identified gene programs with high discriminatory/diagnostic value, including multi-gene signatures that model T/NK cell maturation. Directly measuring these diagnostic programs complements unsupervised analyses.
Enhanced interpretation of immune cell phenotype and function through a rhesus macaque single-cell atlas.
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作者:Mahyari Eisa, Boggy Gregory J, McElfresh G W, Kaza Maanasa, Benjamin Sebastian, Varco-Merth Benjamin, Ojha Sohita, Feltham Shana, Goodwin William, Nkoy Candice, Duell Derick, Selseth Andrea, Bennett Tyler, Barber-Axthelm Aaron, Smedley Jeremy V, Labriola Caralyn S, Axthelm Michael K, Reeves R Keith, Okoye Afam A, Hansen Scott G, Picker Louis J, Bimber Benjamin N
| 期刊: | Cell Genomics | 影响因子: | 9.000 |
| 时间: | 2025 | 起止号: | 2025 May 14; 5(5):100849 |
| doi: | 10.1016/j.xgen.2025.100849 | ||
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