免疫缺陷疾病儿童对肺炎球菌结合疫苗(Prevenar®13)的IgG抗体反应

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Marta Garrido-Jareño, José Miguel Sahuquillo-Arce, Héctor Rodríguez-Vega, Carmen Lloret-Sos, Ana Gil-Brusola, José Luis López-Hontangas, María Nuñez-Beltran, Jordi Tortosa-Carreres, José Ángel García-García, Lourdes Cordón, Leonor Puchades-Carrasco, Carmen Carreras-Gil de Santivañes, Antonio Pineda-Lucena, Javier Pemán-García
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引用次数: 1

摘要

测定抗肺炎球菌荚膜多糖(抗pnps) IgG滴度是对疑似免疫缺陷疾病(ID)患者进行免疫学评估的重要工具,可以降低发病率和死亡率,减少严重感染。回顾性地,我们研究了抗pnps IgG对3种剂量的Prevenar®13的应答、免疫系统成分水平、白细胞群和ID儿童临床数据之间的关系。接种疫苗后至少4周采集血清样本。随后进行多血清型酶联免疫吸附试验(ELISA)。87名儿童(12岁以下)报名参加。原发性免疫缺陷障碍(PID)最为常见(45例),其次是可能性免疫缺陷障碍(POID)(19例)、继发性免疫缺陷障碍(SID)(15例)和混合性免疫缺陷障碍(MID)(8例)。中位年龄为3岁(1.50 ~ 5.33)岁,男性占65%。47例(54%)患者检测到抗pnps IgG(滴度≤50 mg/L)产生不足,特别是MID组,所有患者均接受免疫抑制治疗。PCV13应答者白细胞群水平均值较高,CD4 + /CD8 + T淋巴细胞(p = 0.372, p = 0.014)、CD56 + /CD16 + NK细胞(p = 0.016)差异有统计学意义。既往骨髓移植患者对PCV13反应最差。肺炎球菌IgG抗体滴度(接种后)以及临床和分析标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

IgG antibody response to pneumococcal-conjugated vaccine (Prevenar®13) in children with immunodeficiency disorders.

IgG antibody response to pneumococcal-conjugated vaccine (Prevenar®13) in children with immunodeficiency disorders.

Measurement of anti-pneumococcal capsular polysaccharides (anti-PnPs) IgG titers is an important tool in the immunologic assessment of patients with suspected immunodeficiency disorders (ID) to reduce the morbi-mortality and minimize severe infections. Retrospectively, we studied the relationship among anti-PnPs IgG response to 3 doses of Prevenar®13, levels of immune system components, leukocyte populations, and clinical data in children with ID. Serum samples were collected at least 4 weeks post vaccination. Subsequently, multi-serotype enzyme-linked immunosorbent assay (ELISA) was performed. Eighty-seven children (under 12 years) were enrolled. Primary immunodeficiency disorder (PID) was the most common disorder (45) followed by possible immunodeficiency disorder (POID) (19), secondary immunodeficiency disorder (SID) (15), and mixed immunodeficiency disorder (MID) (8). The median age was 3 (1.50-5.33) years, 65% of patients were male. Deficient production of anti-PnPs IgG (titer ≤ 50 mg/L) was detected in 47 patients (54%), especially in the MID group, all of them under immunosuppressive therapy. In PCV13 responders, the mean of leukocyte population levels was higher with statistically significance differences in CD4 + /CD8 + T lymphocytes (p = 0.372, p = 0.014) and CD56 + /CD16 + NK (p = 0.016). Patients with previous bone marrow transplantation were the worst PCV13 responders. Pneumococcal IgG antibody titers (post-vaccination) along with clinical and analytical markers represented.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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