부산대학교 도서관

Simple Summary: Sex is a factor that affects how the immune system works in both healthy and sick people. There are differences between females and males in various aspects of cancer, such as frequency of diagnosis, treatment response and survival. However, females are often underrepresented in clinical trials that investigate immunological cancer treatments. Further, sex-related differences are rarely studied. Not much is known about how sex affects pancreatic cancer, especially when it comes to the immune system. We looked at cancer tissues and blood samples from pancreatic cancer patients and found that females had a stronger systemic immune response and differential immune responses in the tissue compared to males. We also found that the effects of a specific cancer treatment with the blockade of CXCL12 differed between sexes. These findings show that it is important to consider sex differences when studying pancreatic cancer and immunological treatments. Background: Mounting evidence suggests that sex plays a critical role in various aspects of cancer such as immune responses. However, a male bias exists in human and non-human studies including immunotherapy trials. The role of sex on immune responses in pancreatic ductal adenocarcinoma (PDA) is unclear. Methods: Here, tumor tissues (tumor and stroma separately) and corresponding blood samples from patients with PDA (n = 52) were systematically analyzed by immunohistochemistry and multiplex cytokine measurements and compared by sex. Results: Females showed a stronger systemic immune response with higher levels of CXCL9, IL1B, IL6, IL10 and IL13. Additionally, more peripheral white blood cells were detected in females. In the microenvironment, males showed higher tumoral levels of CXCL12. No differences were detected in the stroma. Females showed a tendency towards an anti-tumoral immune cell profile. CXCL12 blockade indicated a differential microenvironmental effect by sex in an independent immunotherapy trial cohort of patients with PDA (one female, five males). The overall survival did not differ by sex in our cohort. Conclusion: Systemic and local immune responses differ between sexes in PDA. Accordingly, sex-dependent differences need to be considered in human studies and for specific immunological interventions before clinical translation. [ABSTRACT FROM AUTHOR]