Jeffrey Modell Foundation, 780 Third Avenue, 47th Floor, New York City, NY, 10017, USA.
Invitae, San Francisco, CA, USA.
Immunol Res. 2020 Jun;68(3):126-134. doi: 10.1007/s12026-020-09131-x.
Primary immunodeficiencies (PI) are genetic defects of the immune system that result in chronic and often life-threatening infections and/or life-threatening autoimmunity if not diagnosed and treated. Patients with a suspected PI, but without a genetic diagnosis, commonly undergo a diagnostic odyssey that is costly, time-consuming, and arduous. This delay in diagnosis prevents appropriate disease management and treatment, contributing to prolonged suffering and decreased quality of life. Although next generation sequencing (NGS) can provide these patients with relief from such a diagnostic odyssey, it is often unavailable, mainly due to cost and inaccessibility. In January 2019, the Jeffrey Modell Foundation (JMF) launched a free genetic sequencing pilot program for Jeffrey Modell Centers Network (JMCN) patients clinically diagnosed with an underlying PI. A total of 21 sites within the JMCN were invited to participate. JMF collaborated with Invitae, and testing was comprised of Invitae's Primary Immunodeficiency Panel, which currently includes 207 genes. A questionnaire was disseminated to each participating physician to evaluate barriers to access to genetic sequencing and changes in disease management and treatment after testing. One hundred fifty-eight patients and 29 family members were tested in this pilot study. Twenty-one percent of patients with a suspected monogenic disorder received a molecular diagnosis, and others received potentially useful diagnostic leads. Based on the results of genetic sequencing, clinical diagnosis was altered in 45% of patients, disease management was altered in 40%, treatment was altered in 36%, and genetic counseling was altered in 62%. The results of this pilot program demonstrate the utility, cost-efficiency, and critical importance of NGS for PI and make the case for broad scale sequence-based diagnostics for PI patients when requested by expert immunologists.
原发性免疫缺陷 (PI) 是免疫系统的遗传缺陷,如果不进行诊断和治疗,会导致慢性且常常危及生命的感染和/或危及生命的自身免疫。疑似患有 PI 但尚未确诊的患者通常会经历一段代价高昂、耗时费力的诊断探索之旅。这种诊断延迟会妨碍适当的疾病管理和治疗,导致患者遭受更长时间的痛苦和降低生活质量。尽管下一代测序 (NGS) 可以为这些患者提供摆脱这种诊断探索之旅的方法,但由于成本和不可及性,它通常无法获得。2019 年 1 月,杰弗里·莫德尔基金会 (JMF) 为杰弗里·莫德尔中心网络 (JMCN) 中临床诊断为潜在 PI 的患者启动了一项免费的基因测序试点计划。JMCN 中的 21 个地点受邀参加。JMF 与 Invitae 合作,测试由 Invitae 的原发性免疫缺陷Panel 组成,该Panel 目前包含 207 个基因。向每位参与的医生分发了一份问卷,以评估获得基因测序的障碍以及测试后疾病管理和治疗的变化。在这项试点研究中,对 158 名患者和 29 名家属进行了测试。21%的疑似单基因疾病患者获得了分子诊断,其他人获得了潜在有用的诊断线索。根据基因测序的结果,45%的患者的临床诊断发生了改变,40%的患者的疾病管理发生了改变,36%的患者的治疗发生了改变,62%的患者的遗传咨询发生了改变。该试点项目的结果表明,NGS 在 PI 中的实用性、成本效益和至关重要性,并为在专家免疫学家要求时为 PI 患者提供基于序列的广泛诊断提供了依据。