Cross-Reactivity with Self-Antigen Tunes the Functional Potential of Naive B Cells Specific for Foreign Antigens.
Holly R SteachBlair L DeBuysscherAllison SchwartzJim BoonyaratanakornkitMelissa L BakerMarti R TooleyNicholas A PeaseJustin James TaylorPublished in: Journal of immunology (Baltimore, Md. : 1950) (2019)
Upon Ag exposure, naive B cells expressing BCR able to bind Ag can undergo robust proliferation and differentiation that can result in the production of Ab-secreting and memory B cells. The factors determining whether an individual naive B cell will proliferate following Ag encounter remains unclear. In this study, we found that polyclonal naive murine B cell populations specific for a variety of foreign Ags express high levels of the orphan nuclear receptor Nur77, which is known to be upregulated downstream of BCR signaling as a result of cross-reactivity with self-antigens in vivo. Similarly, a fraction of naive human B cells specific for clinically-relevant Ags derived from respiratory syncytial virus and HIV-1 also exhibited an IgMLOW IgD+ phenotype, which is associated with self-antigen cross-reactivity. Functionally, naive B cells expressing moderate levels of Nur77 are most likely to proliferate in vivo following Ag injection. Together, our data indicate that BCR cross-reactivity with self-antigen is a common feature of populations of naive B cells specific for foreign Ags and a moderate level of cross-reactivity primes individual cells for optimal proliferative responses following Ag exposure.
Keyphrases
- hiv infected
- antiretroviral therapy
- quantum dots
- acute lymphoblastic leukemia
- tyrosine kinase
- respiratory syncytial virus
- highly efficient
- human immunodeficiency virus
- visible light
- endothelial cells
- high intensity
- electronic health record
- signaling pathway
- hepatitis c virus
- hiv testing
- cell proliferation
- risk assessment
- climate change
- men who have sex with men
- oxidative stress
- induced pluripotent stem cells
- cell death
- human health
- pluripotent stem cells