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SARS‐CoV‐2‐specific humoral and cellular immunity persists through 9 months irrespective of COVID‐19 severity at hospitalisation
dc.contributor.author | Sandberg, John Tyler | |
dc.contributor.author | Varnaitė, Renata | |
dc.contributor.author | Christ, Wanda | |
dc.contributor.author | Chen, Puran | |
dc.contributor.author | Muvva, Jagadeeswara R | |
dc.contributor.author | Malek, Kimia T | |
dc.contributor.author | García, Marina | |
dc.contributor.author | Dzidic, Majda | |
dc.contributor.author | Folkesson, Elin | |
dc.contributor.author | Skagerberg, Magdalena | |
dc.contributor.author | Ahlén, Gustaf | |
dc.contributor.author | Frelin, Lars | |
dc.contributor.author | Sällberg, Matti | |
dc.contributor.author | Eriksson, Lars | |
dc.contributor.author | Rooyackers, Olav | |
dc.contributor.author | Sönnerborg, Anders | |
dc.contributor.author | Buggert, Marcus | |
dc.contributor.author | Björkström, Niklas K | |
dc.contributor.author | Aleman, Soo | |
dc.contributor.author | Strålin, Kristoffer | |
dc.contributor.author | Klingström, Jonas | |
dc.contributor.author | Ljunggren, Hans Gustaf | |
dc.contributor.author | Blom, Kim | |
dc.contributor.author | Karolinska COVID-19 Study Group | |
dc.contributor.author | Akber, Muhammad | |
dc.contributor.author | Berglin, L | |
dc.contributor.author | Bergsten, Helena | |
dc.contributor.author | Björkström, Niklas | |
dc.contributor.author | Brighenti, Susanna | |
dc.contributor.author | Brownlie, Demmi | |
dc.contributor.author | Butrym, Marta | |
dc.contributor.author | Chambers, BJ | |
dc.contributor.author | Cornillet, Martin | |
dc.contributor.author | Cuapio, Angelica | |
dc.contributor.author | Díaz Lozano, Isabel María | |
dc.contributor.author | Dillner, L | |
dc.contributor.author | Emgård, Johanna | |
dc.contributor.author | Flodström Tullberg, Malin | |
dc.contributor.author | Färnert, A | |
dc.contributor.author | Gao, Y | |
dc.contributor.author | Glans, H | |
dc.contributor.author | Gorin, Jean Baptiste | |
dc.contributor.author | Grip, J | |
dc.contributor.author | Haroun Izquierdo, Álvaro | |
dc.contributor.author | Henriksson, E | |
dc.contributor.author | Hertwig, L | |
dc.contributor.author | Kalsum, S | |
dc.contributor.author | Kammann, Tobias | |
dc.contributor.author | Kokkinou, E | |
dc.contributor.author | Kvedaraite, E | |
dc.contributor.author | Loreti, MG | |
dc.contributor.author | Lourda, M | |
dc.contributor.author | Malmberg, KJ | |
dc.contributor.author | Marquardt, N | |
dc.contributor.author | Maucourant, C | |
dc.contributor.author | Mårtensson, J | |
dc.contributor.author | Michaëlsson, J | |
dc.contributor.author | Mjösberg, J | |
dc.contributor.author | Moll, K | |
dc.contributor.author | Nauclér, P | |
dc.contributor.author | Norrby‐Teglund, Anna | |
dc.contributor.author | Palma Medina, Laura | |
dc.contributor.author | Parrot, T | |
dc.contributor.author | Perez‐Potti, André | |
dc.contributor.author | Persson, BP | |
dc.contributor.author | Radler, L | |
dc.contributor.author | Ringqvist, E | |
dc.contributor.author | Rivera Ballesteros, Olga | |
dc.contributor.author | Sandberg, K | |
dc.contributor.author | Sekine, Takuya | |
dc.contributor.author | Sohlberg, E | |
dc.contributor.author | Soini, T | |
dc.contributor.author | Svensson, M | |
dc.contributor.author | Tynell, J | |
dc.contributor.author | Unge, C | |
dc.contributor.author | von Kries, A | |
dc.contributor.author | Wullimann, David | |
dc.contributor.author | Gredmark-Russ, Sara | |
dc.contributor.author | Karolinska COVID-19 Study Group | |
dc.date.accessioned | 2024-02-12T08:06:24Z | |
dc.date.available | 2024-02-12T08:06:24Z | |
dc.date.issued | 2021 | |
dc.identifier.uri | http://hdl.handle.net/10952/7331 | |
dc.description.abstract | Objectives Humoral and cellular immunity to SARS-CoV-2 following COVID-19 will likely contribute to protection from reinfection or severe disease. It is therefore important to characterise the initiation and persistence of adaptive immunity to SARS-CoV-2 amidst the ongoing pandemic. Methods Here, we conducted a longitudinal study on hospitalised moderate and severe COVID-19 patients from the acute phase of disease into convalescence at 5 and 9 months post-symptom onset. Utilising flow cytometry, serological assays as well as B cell and T cell FluoroSpot assays, we assessed the magnitude and specificity of humoral and cellular immune responses during and after human SARS-CoV-2 infection. Results During acute COVID-19, we observed an increase in germinal centre activity, a substantial expansion of antibody-secreting cells and the generation of SARS-CoV-2-neutralising antibodies. Despite gradually decreasing antibody levels, we show persistent, neutralising antibody titres as well as robust specific memory B cell responses and polyfunctional T cell responses at 5 and 9 months after symptom onset in both moderate and severe COVID-19 patients. Conclusion Our findings describe the initiation and, importantly, persistence of cellular and humoral SARS-CoV-2-specific immunological memory in hospitalised COVID-19 patients long after recovery, likely contributing towards protection against reinfection. | es |
dc.language.iso | en | es |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.title | SARS‐CoV‐2‐specific humoral and cellular immunity persists through 9 months irrespective of COVID‐19 severity at hospitalisation | es |
dc.type | article | es |
dc.rights.accessRights | openAccess | es |
dc.journal.title | Clinical & translational immunology | es |
dc.volume.number | 10 | es |
dc.issue.number | 7 | es |
dc.description.discipline | Medicina | es |
dc.identifier.doi | https://doi.org/10.1002/cti2.1306 | es |