Cieri Nicoletta, Hookeri Nidhi, Stromhaug Kari, Li Liang, Keating Julia, Díaz-Fernández Paula, Gómez-García de Soria Valle, Stevens Jonathan, Kfuri-Rubens Raphael, Shao Yiren, Kooshesh Kameron A, Powell Kaila, Ji Helen, Hernandez Gabrielle M, Abelin Jennifer, Klaeger Susan, Forman Cleo, Clauser Karl R, Sarkizova Siranush, Braun David A, Penter Livius, Kim Haesook T, Lane William J, Oliveira Giacomo, Kean Leslie S, Li Shuqiang, Livak Kenneth J, Carr Steven A, Keskin Derin B, Muñoz-Calleja Cecilia, Ho Vincent T, Ritz Jerome, Soiffer Robert J, Neuberg Donna, Stewart Chip, Getz Gad, Wu Catherine J
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, MA, USA.
Nat Biotechnol. 2024 Aug 21. doi: 10.1038/s41587-024-02348-3.
T cell alloreactivity against minor histocompatibility antigens (mHAgs)-polymorphic peptides resulting from donor-recipient (D-R) disparity at sites of genetic polymorphisms-is at the core of the therapeutic effect of allogeneic hematopoietic cell transplantation (allo-HCT). Despite the crucial role of mHAgs in graft-versus-leukemia (GvL) and graft-versus-host disease (GvHD) reactions, it remains challenging to consistently link patient-specific mHAg repertoires to clinical outcomes. Here we devise an analytic framework to systematically identify mHAgs, including their detection on HLA class I ligandomes and functional verification of their immunogenicity. The method relies on the integration of polymorphism detection by whole-exome sequencing of germline DNA from D-R pairs with organ-specific transcriptional- and proteome-level expression. Application of this pipeline to 220 HLA-matched allo-HCT D-R pairs demonstrated that total and organ-specific mHAg load could independently predict the occurrence of acute GvHD and chronic pulmonary GvHD, respectively, and defined promising GvL targets, confirmed in a validation cohort of 58 D-R pairs, for the prevention or treatment of post-transplant disease recurrence.
针对次要组织相容性抗原(mHAgs)——由遗传多态性位点上供体-受体(D-R)差异产生的多态性肽段——的T细胞同种异体反应性是异基因造血细胞移植(allo-HCT)治疗效果的核心。尽管mHAgs在移植物抗白血病(GvL)和移植物抗宿主病(GvHD)反应中起关键作用,但将患者特异性mHAg库与临床结果持续关联起来仍然具有挑战性。在此,我们设计了一个分析框架,以系统地鉴定mHAgs,包括在HLA I类配体组上对它们的检测以及对其免疫原性的功能验证。该方法依赖于将来自D-R对的种系DNA全外显子测序的多态性检测与器官特异性转录组和蛋白质组水平的表达相结合。将此流程应用于220对HLA匹配的allo-HCT D-R对,结果表明总的和器官特异性的mHAg负荷分别能够独立预测急性GvHD和慢性肺部GvHD的发生,并确定了有前景的GvL靶点,在一个由58对D-R对组成的验证队列中得到证实,可用于预防或治疗移植后疾病复发。