Identification of a spike-specific CD8+ T cell epitope following vaccination against the Middle East respiratory syndrome coronavirus in humans
© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America..
Licensed vaccines against the Middle East respiratory syndrome coronavirus (MERS-CoV), an emerging pathogen of concern, are lacking. The Modified Vaccinia virus Ankara vector-based vaccine MVA-MERS-S, expressing the MERS-CoV-spike glycoprotein (MERS-S), is one of three candidate vaccines in clinical development and elicits robust humoral and cellular immunity. Here, we identified for the first time a MERS-S-specific CD8+ T-cell epitope in an HLA-A*03:01/HLA-B*35:01-positive vaccinee using a screening assay, intracellular cytokine staining, and in silico epitope prediction. As evidence from MERS-CoV infection suggests a protective role of long-lasting CD8+ T-cell responses, the identification of epitopes will facilitate longitudinal analyses of vaccine-induced T-cell immunity.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
---|---|
Enthalten in: |
The Journal of infectious diseases - (2024) vom: 09. Jan. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Harrer, Caroline E [VerfasserIn] |
---|
Links: |
---|
Themen: |
CD8+ T cells |
---|
Anmerkungen: |
Date Revised 09.01.2024 published: Print-Electronic Citation Status Publisher |
---|
doi: |
10.1093/infdis/jiad612 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM366858076 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM366858076 | ||
003 | DE-627 | ||
005 | 20240114233613.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240114s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1093/infdis/jiad612 |2 doi | |
028 | 5 | 2 | |a pubmed24n1255.xml |
035 | |a (DE-627)NLM366858076 | ||
035 | |a (NLM)38195212 | ||
035 | |a (PII)jiad612 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Harrer, Caroline E |e verfasserin |4 aut | |
245 | 1 | 0 | |a Identification of a spike-specific CD8+ T cell epitope following vaccination against the Middle East respiratory syndrome coronavirus in humans |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 09.01.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status Publisher | ||
520 | |a © The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. | ||
520 | |a Licensed vaccines against the Middle East respiratory syndrome coronavirus (MERS-CoV), an emerging pathogen of concern, are lacking. The Modified Vaccinia virus Ankara vector-based vaccine MVA-MERS-S, expressing the MERS-CoV-spike glycoprotein (MERS-S), is one of three candidate vaccines in clinical development and elicits robust humoral and cellular immunity. Here, we identified for the first time a MERS-S-specific CD8+ T-cell epitope in an HLA-A*03:01/HLA-B*35:01-positive vaccinee using a screening assay, intracellular cytokine staining, and in silico epitope prediction. As evidence from MERS-CoV infection suggests a protective role of long-lasting CD8+ T-cell responses, the identification of epitopes will facilitate longitudinal analyses of vaccine-induced T-cell immunity | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a CD8+ T cells | |
650 | 4 | |a MERS-CoV | |
650 | 4 | |a MVA | |
650 | 4 | |a epitope | |
650 | 4 | |a vaccine | |
650 | 4 | |a viral vector | |
700 | 1 | |a Mayer, Leonie |e verfasserin |4 aut | |
700 | 1 | |a Fathi, Anahita |e verfasserin |4 aut | |
700 | 1 | |a Lassen, Susan |e verfasserin |4 aut | |
700 | 1 | |a Ly, My L |e verfasserin |4 aut | |
700 | 1 | |a Zinser, Madeleine E |e verfasserin |4 aut | |
700 | 1 | |a Wolf, Timo |e verfasserin |4 aut | |
700 | 1 | |a Becker, Stephan |e verfasserin |4 aut | |
700 | 1 | |a Sutter, Gerd |e verfasserin |4 aut | |
700 | 1 | |a Dahlke, Christine |e verfasserin |4 aut | |
700 | 1 | |a Addo, Marylyn M |e verfasserin |4 aut | |
700 | 0 | |a MVA-MERS-S Study Group |e verfasserin |4 aut | |
700 | 1 | |a Bartels, Etienne |e investigator |4 oth | |
700 | 1 | |a Gundlach, Swantje |e investigator |4 oth | |
700 | 1 | |a Haagmanns, Bart |e investigator |4 oth | |
700 | 1 | |a Hesterkamp, Thomas |e investigator |4 oth | |
700 | 1 | |a Koch, Till |e investigator |4 oth | |
700 | 1 | |a Krähling, Verena |e investigator |4 oth | |
700 | 1 | |a Poetsch, Joseph |e investigator |4 oth | |
700 | 1 | |a Schmiedel, Stefan |e investigator |4 oth | |
700 | 1 | |a Volz, Asisa |e investigator |4 oth | |
773 | 0 | 8 | |i Enthalten in |t The Journal of infectious diseases |d 1945 |g (2024) vom: 09. Jan. |w (DE-627)NLM000005819 |x 1537-6613 |7 nnns |
773 | 1 | 8 | |g year:2024 |g day:09 |g month:01 |
856 | 4 | 0 | |u http://dx.doi.org/10.1093/infdis/jiad612 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |j 2024 |b 09 |c 01 |