Antiapoptotic serine protease inhibitors contribute to survival of allergenic TH2 cells

• Published in: Journal of allergy and clinical immunology 2018-08, Vol.142 (2), p.569-581.e5
• Main Authors: Shamji, Mohamed H., Temblay, Jeff N., Cheng, Wei, Byrne, Susan M., Macfarlane, Ellen, Switzer, Amy R., Francisco, Natalia D.C., Olexandra, Fedina, Jacubczik, Fabian, Durham, Stephen R., Ashton-Rickardt, Philip G.
• Format: Article
• Language: English
• Subjects: apoptosis; grass pollen allergy; memory; TH2 cells
• ISSN: 0091-6749; 1097-6825; 1097-6825
• DOI: 10.1016/j.jaci.2017.07.055

The mechanisms that regulate maintenance of persistent TH2 cells and potentiate allergic inflammation are not well understood. The function of serine protease inhibitor 2A (Spi2A) was studied in mouse TH2 cells, and the serine protease inhibitor B3 (SERPINB3) and SERPINB4 genes were studied in TH2 cells from patients with grass pollen allergy. Spi2A-deficient TH2 cells were studied in in vitro culture or in vivo after challenge of Spi2A knockout mice with ovalbumin in alum. Expression of SERPINB3 and SERPINB4 mRNA was measured in in vitro–cultured TH2 cells and in ex vivo CD27−CD4+ cells and innate lymphoid cell (ILC) 2 from patients with grass pollen allergy by using quantitative PCR. SERPINB3 and SERPINB4 mRNA levels were knocked down in cultured CD27−CD4+ cells with small hairpin RNA. There were lower levels of in vitro–polarized TH2 cells from Spi2A knockout mice (P