Yang Xiaoqi, Fox Alisa, DeCarlo Claire, Powell Rebecca L R
Division of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Breastfeed Med. 2024 Dec;19(12):974-979. doi: 10.1089/bfm.2024.0257. Epub 2024 Oct 2.
JYNNEOS is a nonreplicating modified vaccinia Ankara vaccine currently licensed to prevent monkeypox infection, and its milk immunogenicity remains unstudied. Investigate the human milk immunogenicity of the JYNNEOS vaccine in one individual and examine the milk for evidence of vaccine components. Immunogenicity of milk and plasma samples were tested by Luminex assays against Vaccinia antigens, and vaccine components were tested using PCR and sandwich ELISA. Plasma antibody (Ab) response increased up to 3.7-fold in immunoglobulin G (IgG) titer and 1.4-fold in IgA compared with baseline, confirming vaccine immunogenicity in this participant 2 weeks post dose 2. Specific plasma IgG remained 1.2- to 1.7-fold above baseline 12 weeks post dose 2, while IgA returned to baseline levels. Notably, the milk response exhibited unique kinetics, particularly for IgA. Milk IgA against all three antigens increased 0.9- to 2.2-fold 2 weeks post dose 2, reaching a peak titer increase of 1.1- to 2.7-fold at 12 weeks post dose 2. Secretory (s) Ab levels increased to 1.1- to 2-fold at 2 weeks post dose 2 and reached a peak of 2- to 3.2-fold increase at the 12-week time point. Importantly, IgA and sAb responses in milk exhibited correlation, suggesting most milk IgA was sIgA. Notably, no vaccine components (VACV protein or DNA) were detected in the milk samples. These data suggest that the milk Ab response to this intradermal (ID) VACV-based vaccine is distinct from that observed systemically, indicating a unique mucosal immune response and highlighting its potential to elicit protective long-lasting sIgA. This case report provides strong evidence for inclusion of this vaccine platform in future studies of maternal vaccines aimed to elicit a protective milk Ab response.
JYNNEOS是一种非复制型改良安卡拉痘苗病毒疫苗,目前已获许可用于预防猴痘感染,但其在母乳中的免疫原性尚未得到研究。本研究调查了一名个体母乳中JYNNEOS疫苗的免疫原性,并检测母乳中疫苗成分的证据。通过Luminex检测法针对痘苗抗原检测母乳和血浆样本的免疫原性,并使用PCR和夹心ELISA检测疫苗成分。与基线相比,血浆抗体(Ab)反应在免疫球蛋白G(IgG)滴度上增加了3.7倍,在IgA上增加了1.4倍,证实了该参与者在第2剂接种后2周疫苗具有免疫原性。在第2剂接种后12周,特异性血浆IgG仍比基线高1.2至1.7倍,而IgA恢复到基线水平。值得注意的是,母乳反应呈现出独特的动力学,尤其是对于IgA。针对所有三种抗原的母乳IgA在第2剂接种后2周增加了0.9至2.2倍,在第2剂接种后12周达到峰值滴度增加1.1至2.7倍。分泌型(s)Ab水平在第2剂接种后2周增加到1.1至2倍,并在12周时间点达到峰值增加2至3.2倍。重要的是,母乳中的IgA和sAb反应呈现相关性,表明大多数母乳IgA是分泌型IgA(sIgA)。值得注意的是,在母乳样本中未检测到疫苗成分(痘苗病毒蛋白或DNA)。这些数据表明,母乳对这种基于皮内(ID)痘苗病毒的疫苗的Ab反应与全身观察到的反应不同,表明存在独特的黏膜免疫反应,并突出了其引发保护性长效sIgA的潜力。本病例报告为将该疫苗平台纳入未来旨在引发保护性母乳Ab反应的母体疫苗研究提供了有力证据。