Evolutionary analysis reveals repeated diversification events in immune metabolic pathways

The human immune system is a complex, multifunctional network essential for host defense, tumor surveillance, and tissue repair. While conventionally divided into rapid-response innate immunity and antigen-specific adaptive immunity with memory, both modules operate synergistically through dynamic metabolic interactions that fuel immune responses. Although host-pathogen coevolution is recognized as a major evolutionary driver, the establishment scenario of immune metabolic pathways remains poorly characterized. Crucially, a systematic understanding of how the emergence of vertebrate malignancy can influence immune adaptations is needed. We analyzed 1,063 genes from 21 KEGG Pathway immune metabolic pathways and 1,124 cancer-associated genes from OncoKB/COSMIC. Evolutionary rooting was performed using the R package GeneBridge, inferring the most probable origins for each Cluster of Orthologous Genes (COG) across a 476-species eukaryotic phylogeny. Four clades showed significant immune orthologous groups (OGs) emergence: Metamonada, SAR, Choanoflagellata, and Actinopterygii. While cancer OGs diversified primarily during multicellular organism origins, immune OGs exhibited multiple diversification peaks, most prominently during jawed vertebrate emergence. Our findings demonstrate that human immune metabolic pathways underwent recurrent adaptive events during evolution, with marked complexity escalation in jawed vertebrates. We propose that malignant neoplasm emergence, coupled with epithelial-immune coevolution, served as complementary selective pressure driving progressive refinement of vertebrate immune mechanisms.