Immune cell subsets in interface cutaneous immune-related adverse events associated with anti-PD-1 therapy resemble acute graft versus host disease more than lichen planus Journal Article


Authors: Cruz, G. E. A.; Kaunitz, G.; Stein, J. E.; Sander, I.; Hollmann, T.; Cottrell, T. R.; Taube, J. M.; Sunshine, J. C.
Article Title: Immune cell subsets in interface cutaneous immune-related adverse events associated with anti-PD-1 therapy resemble acute graft versus host disease more than lichen planus
Abstract: Background Checkpoint immunotherapy is frequently associated with cutaneous immune-related adverse events (cirAEs), and among those, the most common subtype shows interface reaction patterns that have been likened to lichen planus (LP); however, cutaneous acute graft versus host disease (aGVHD) may be a closer histopathologic comparator. We used quantitative pathology to compare the immunologic composition of anti-PD-1-associated interface reactions to LP and aGVHD to assess for similarities and differences between these cutaneous eruptions. Methods Immunohistochemistry for CD4, CD8, CD68, PD-1, and PD-L1 was performed on formalin-fixed paraffin-embedded tissue from patients with anti-PD-1 interface cirAEs (n = 4), LP (n = 9), or aGVHD (n = 5). Densities of immune cell subsets expressing each marker were quantified using the HALO image analysis immune cell module. Plasma cell and eosinophil density were quantified on routine H&E slides. Results Specimens from patients with anti-PD-1 interface cirAEs showed equivalent total cell densities and immune cell composition to those with aGVHD. Patients with LP showed higher total immune cell infiltration, higher absolute T-cell densities, increased CD8 proportion, and reduced histiocytic component. The cases with the highest plasma cell counts were all anti-PD-1 interface cirAEs and aGVHD. Conclusion The composition of immune cell subsets in anti-PD-1 interface cirAEs more closely resembles the immune response seen in aGVHD than LP within our cohort. This warrants a closer look via advanced analytics and may have implications for shared pathogenesis and potential treatment options.
Keywords: lichen planus; gvhd; pd-1; patient; features; t-cells; events; checkpoint blockade; dermatological toxicities; death 1; graft versus host disease; immune-related adverse; cutaneous eruptions; immunologic markers; eruptions
Journal Title: Journal of Cutaneous Pathology
Volume: 49
Issue: 8
ISSN: 0303-6987
Publisher: John Wiley & Sons  
Date Published: 2022-08-01
Start Page: 701
End Page: 708
Language: English
ACCESSION: WOS:000795795900001
DOI: 10.1111/cup.14242
PROVIDER: wos
PMCID: PMC9305991
PUBMED: 35445765
Notes: Article -- Source: Wos
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  1. Travis Jason Hollmann
    126 Hollmann