Impaired HPV-specific T-cell response in juvenile-onset recurrent respiratory papillomatosis patients

被引:6
|
作者
Xi, Yue [1 ,4 ]
Wang, Wei [1 ]
Wang, Hua [2 ]
Wang, Xiaolin [1 ]
Zhang, Jie [2 ]
Zhao, Jing [2 ]
Wang, Guixiang [2 ]
Gui, Jingang [1 ]
Ni, Xin [1 ,2 ,3 ]
机构
[1] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Beijing Pediat Res Inst,Lab Tumor Immunol, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Childrens Hosp, Dept Otolaryngol Head & Neck Surg, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Key Lab Pediat Dis Otolaryngol Head & Nec, Beijing Pediat Res Inst, Beijing Childrens Hosp, Beijing, Peoples R China
[4] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Nephrol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
JORRP; HPV; T-cell response; Cytokine; Immune imbalance; NATIONAL REGISTRY; EXPRESSION;
D O I
10.1016/j.clim.2022.109046
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunologic dysfunction is one of the most important mechanisms underlying the initiation and development of JORRP. The study aimed to explore whether HPV-specific T-cell response was impaired in JORRP patients. We found JORRP patients had a Th2-biased cytokine profile correlated with disease severity in peripheral system. JORRP patients had an increased memory T cells and a reduced naive T cells in circulation. Upon HPV6/11 antigens stimulation, T cells from JORRP patients exhibited a greater activation profile. Of note, JORRP patients presented with a greater number of IL-10- and IL-4-secreting HPV6/11 antigen responding cells than that of IFN-gamma and TNF-alpha secreting responders. Furthermore, in response to HPV6/11 antigen stimulation, JORRP patients showed a reduced level of cell proliferation, an increased level of apoptosis and higher percentage of the differentiated T cells expressing the replicative senescent cell marker CD57. Impaired HPV-specific T-cell responses could be partly responsible for JORRP development.
引用
收藏
页数:8
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