Persistent immune imprinting after XBB.1.5 COVID vaccination in humans.

التفاصيل البيبلوغرافية
العنوان: Persistent immune imprinting after XBB.1.5 COVID vaccination in humans.
المؤلفون: Tortorici MA; Department of Biochemistry, University of Washington, Seattle, WA, USA., Addetia A; Department of Biochemistry, University of Washington, Seattle, WA, USA., Seo AJ; Department of Biochemistry, University of Washington, Seattle, WA, USA., Brown J; Department of Biochemistry, University of Washington, Seattle, WA, USA., Sprouse KR; Department of Biochemistry, University of Washington, Seattle, WA, USA., Logue J; Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA, USA., Clark E; Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA, USA., Franko N; Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA, USA., Chu H; Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA, USA., Veesler D; Department of Biochemistry, University of Washington, Seattle, WA, USA.; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
المصدر: BioRxiv : the preprint server for biology [bioRxiv] 2023 Nov 30. Date of Electronic Publication: 2023 Nov 30.
نوع المنشور: Preprint
اللغة: English
بيانات الدورية: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE
مستخلص: Immune imprinting - also known as 'original antigenic sin' - describes how the first exposure to a virus shapes the immunological outcome of subsequent exposures to antigenically related strains. SARS-CoV-2 Omicron breakthrough infections and bivalent COVID-19 vaccination were shown to primarily recall cross-reactive memory B cells and antibodies induced by prior mRNA vaccination with the Wuhan-Hu-1 spike rather than priming naive B cells that recognize Omicron-specific epitopes. These findings underscored a strong immune imprinting resulting from repeated Wuhan-Hu-1 spike exposures. To understand if immune imprinting can be overcome, we investigated memory and plasma antibody responses after administration of the updated XBB.1.5 COVID mRNA vaccine booster. Our data show that the XBB.1.5 booster elicits neutralizing antibody responses against current variants that are dominated by recall of pre-existing memory B cells previously induced by the Wuhan-Hu-1 spike. These results indicate that immune imprinting persists even after multiple exposures to Omicron spikes through vaccination and infection, including post XBB.1.5 spike booster mRNA vaccination, which will need to be considered to guide the design of future vaccine boosters.
التعليقات: Update in: Immunity. 2024 Mar 8;:. (PMID: 38490197)
References: Nature. 2021 Oct;598(7880):342-347. (PMID: 34464958)
Nature. 2023 Feb;614(7948):521-529. (PMID: 36535326)
Nature. 2023 Sep;621(7979):592-601. (PMID: 37648855)
Nature. 2021 Jun;594(7862):253-258. (PMID: 33873199)
iScience. 2023 Jan 20;26(1):105726. (PMID: 36507220)
Science. 2020 Sep 18;369(6510):1501-1505. (PMID: 32703906)
Sci Immunol. 2022 Sep 16;7(75):eabq2427. (PMID: 35653438)
Nature. 2021 Feb;590(7847):630-634. (PMID: 33276369)
Cell Host Microbe. 2020 Sep 9;28(3):475-485.e5. (PMID: 32735849)
Cell. 2022 Jun 23;185(13):2279-2291.e17. (PMID: 35700730)
Nature. 2022 Apr;604(7904):141-145. (PMID: 35168246)
N Engl J Med. 2022 Oct 6;387(14):1279-1291. (PMID: 36112399)
Nature. 2023 Nov 22;:. (PMID: 37993710)
J Virol. 2010 Apr;84(7):3210-9. (PMID: 20071581)
Nature. 2022 Jul;607(7917):128-134. (PMID: 35447027)
Cell. 2020 Apr 16;181(2):281-292.e6. (PMID: 32155444)
Science. 2022 Nov 11;378(6620):619-627. (PMID: 36264829)
Nat Med. 2023 Jan;29(1):247-257. (PMID: 36265510)
Lancet Microbe. 2023 Aug;4(8):e569. (PMID: 37141905)
Nat Med. 2021 Jul;27(7):1205-1211. (PMID: 34002089)
Science. 2021 Feb 5;371(6529):. (PMID: 33408181)
Sci Transl Med. 2021 Jun 30;13(600):. (PMID: 34103407)
Science. 2021 Sep 17;373(6561):eabj0299. (PMID: 34529476)
Sci Immunol. 2022 Dec 23;7(78):eadf1421. (PMID: 36356052)
Cell. 2020 Nov 12;183(4):1024-1042.e21. (PMID: 32991844)
Nature. 2021 Jul;595(7867):426-431. (PMID: 34126625)
معلومات مُعتمدة: 75N93022C00036 United States AI NIAID NIH HHS; DP1 AI158186 United States AI NIAID NIH HHS; P01 AI167966 United States AI NIAID NIH HHS
تواريخ الأحداث: Date Created: 20231211 Latest Revision: 20240410
رمز التحديث: 20240411
مُعرف محوري في PubMed: PMC10705481
DOI: 10.1101/2023.11.28.569129
PMID: 38076876
قاعدة البيانات: MEDLINE
الوصف
DOI:10.1101/2023.11.28.569129