Zuzolo Jenna, Zulfiqar Muhammad F, Spoelhof Brian, Revell Rebecca, Patrie James T, Borish Larry, Lawrence Monica G
Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia.
University of Virginia School of Medicine, Charlottesville, Virginia.
Ann Allergy Asthma Immunol. 2025 Mar;134(3):279-283. doi: 10.1016/j.anai.2024.12.011. Epub 2024 Dec 15.
Humoral immune disorders such as common variable immunodeficiency and specific antibody deficiency are prevalent in clinical practice and require accurate functional testing of humoral immunity for diagnosis and to guide treatment approach. Traditionally, the 23-valent pneumococcal polysaccharide vaccine (PPSV23) has been used to assess polysaccharide antibody responses by measuring pre- and post-vaccination pneumococcal titers. However, the recent introduction of pneumococcal conjugate vaccines (PCVs), such as PCV13, PCV15, and PCV20, into the childhood and adult vaccine schedules has significantly reduced the number of unique serotypes available for testing and in turn has complicated the evaluation process. We retrospectively analyzed serotype-specific antibody responses in patients aged 2 to 65 years who received PPSV23 at the University of Virginia Health System to compare diagnostic outcomes using all 23 serotypes vs the limited number of unique serotypes not included in previous PCVs-11 serotypes for PCV13 recipients and 4 for PCV20 recipients. Our findings reveal that although previous PCVs mean that there is a reduced number of serotypes available for interpretation, PPSV23 testing maintains diagnostic accuracy between 81% and 84%. Despite limitations, the use of PPSV23 remains a valuable tool for identifying patients with clinically significant humoral immune deficiencies. In the future, alternative diagnostic approaches such as Salmonella typhi polysaccharide vaccine response and opsonophagocytosis assays may become more frequently used as part of the evaluation of humoral immune disorders.
常见可变免疫缺陷和特异性抗体缺陷等体液免疫紊乱在临床实践中很常见,需要对体液免疫进行准确的功能测试以进行诊断并指导治疗方法。传统上,23价肺炎球菌多糖疫苗(PPSV23)一直用于通过测量接种疫苗前后的肺炎球菌滴度来评估多糖抗体反应。然而,最近将肺炎球菌结合疫苗(PCV),如PCV13、PCV15和PCV20,纳入儿童和成人疫苗接种计划,显著减少了可用于检测的独特血清型数量,进而使评估过程变得复杂。我们回顾性分析了在弗吉尼亚大学健康系统接受PPSV23的2至65岁患者的血清型特异性抗体反应,以比较使用所有23种血清型与先前PCV中未包含的有限数量独特血清型(PCV13接种者为11种血清型,PCV20接种者为4种血清型)的诊断结果。我们的研究结果表明,尽管先前的PCV意味着可用于解读的血清型数量减少,但PPSV23检测的诊断准确率仍保持在81%至84%之间。尽管存在局限性,但使用PPSV23仍然是识别具有临床显著体液免疫缺陷患者的宝贵工具。未来,替代诊断方法,如伤寒沙门氏菌多糖疫苗反应和调理吞噬作用测定,可能会更频繁地用作体液免疫紊乱评估的一部分。