Low Baseline Pneumococcal Antibody Titers Predict Specific Antibody Deficiency, Increased Upper Respiratory Infections, and Allergy Sensitization.

IF 2.3 Q1 OTORHINOLARYNGOLOGY Allergy & Rhinology Pub Date : 2020-01-22 eCollection Date: 2020-01-01 DOI:10.1177/2152656719900338
Charles H Song, Dennys Estevez, Diana Chernikova, Francesca Hernandez, Rie Sakai-Bizmark, Richard Stiehm
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引用次数: 6

Abstract

Background: Inadequate titers of pneumococcal antibody (PA) are commonly present among patients with recurrent respiratory infections.

Objective: We sought to determine the effect of the degree of inadequacy in baseline PA titers on the subsequent polysaccharide vaccine response, the incidence of sinusitis, and allergic conditions.

Methods: A total of 313 patients aged 6 to 70 years with symptoms of recurrent respiratory infections were classified by baseline-pPA (percentage of protective [≥1.3 µg/mL] PA serotypes/total tested serotypes) and postvaccination pPA (post-pPA): Group A (adequate baseline-pPA), Group B (inadequate baseline-pPA, adequate post-pPA, responders), and Group C (inadequate baseline-pPA, inadequate postpPA, nonresponders, specific antibody deficiency [SAD]). Immunity against Streptococcus pneumoniae was defined as adequate when the pPA was ≥70%. Each group and combined groups, Group AB (inadequate baseline-pPA), and Group BC (adequate post-pPA) were analyzed for demographics, history of sinusitis, recurrent sinusitis in the following year, allergic conditions, and association with inadequate individual serotype titers.

Results: Over 80% of patients with respiratory symptoms had inadequate baseline-pPA. Baseline-pPA and SAD prevalence are inversely related (odds ratio = 2.02, 95% CI: 1.15-3.57, P = .01). Inadequate serotype 3 antibody titer is highly associated with SAD (odds ratio = 2.02, 96% CI: 1.61-5.45, P < .01). The groups with inadequate pPA (Group B and C, or BC) had significantly higher percentage of patients with chronic rhinosinusitis (P < .001), allergic sensitization, and allergic rhinitis (P < .05). Group A contained higher percentage of patients with recurrent upper airway infections (P < .001).

Conclusion: Low baseline-pPA and low antibody titers to serotype 3 are highly associated with SAD, increased incidence of respiratory infections including CRS and allergic conditions.

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低基线肺炎球菌抗体滴度预测特异性抗体缺乏、上呼吸道感染增加和过敏致敏。
背景:肺炎球菌抗体(PA)滴度不足通常存在于反复呼吸道感染的患者中。目的:我们试图确定基线PA滴度不足程度对随后的多糖疫苗应答、鼻窦炎发生率和过敏状况的影响。方法:共有313例6 ~ 70岁的复发性呼吸道感染患者,根据基线-pPA(保护性[≥1.3µg/mL] PA血清型/总检测血清型百分比)和接种后pPA(后pPA)进行分类:A组(基线-pPA充足)、B组(基线-pPA不足、后pPA充足、应答)和C组(基线-pPA不足、后pPA不足、无应答、特异性抗体缺乏[SAD])。当pPA≥70%时,对肺炎链球菌的免疫被定义为足够。分析每组和联合组、AB组(基线- ppa不足)和BC组(ppa后充足)的人口统计学、鼻窦炎史、次年鼻窦炎复发、过敏情况以及与个体血清型滴度不足的关系。结果:超过80%的呼吸道症状患者基线ppa不足。基线- ppa和SAD患病率呈负相关(优势比= 2.02,95% CI: 1.15-3.57, P = 0.01)。血清3型抗体滴度不足与SAD高度相关(优势比= 2.02,96% CI: 1.61 ~ 5.45, P P P P P P)结论:低基线- ppa和血清3型抗体滴度低与SAD、呼吸道感染(包括CRS)发生率增加和过敏性疾病高度相关。
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来源期刊
Allergy & Rhinology
Allergy & Rhinology OTORHINOLARYNGOLOGY-
CiteScore
3.30
自引率
4.50%
发文量
11
审稿时长
15 weeks
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