For example, recombinant IL‐8 administration in large animals increased neutrophil infiltration while reducing uterine inflammation.[48] Similarly, intravenous administration of radiolabeled IL‐8 led to selective accumulation at infection sites without affecting peripheral lymphocyte populations.[49] Collectively, these findings suggest that the immunomodulatory effects of IL‐8 are highly context‐dependent. Here, CXCL8 is linked to infection.