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Distinguishing features of long COVID identified through immune profiling

Open access
Klein, Jon, Wood, Jamie, Jaycox, Jillian R., Dhodapkar, Rahul M., Lu, Peiwen, Gehlhausen, Jeff R., Tabachnikova, Alexandra, Greene, Kerrie, Tabacof, Laura, Malik, Amyn A., Silva Monteiro, Valter, Silva, Julio, Kamath, Kathy, Zhang, Minlu, Dhal, Abhilash, Ott, Isabel M., Valle, Gabrielee, Peña-Hernández, Mario, Mao, Tianyang, Bhattacharjee, Bornali, Takahashi, Takehiro, Lucas, Carolina, Song, Eric, McCarthy, Dayna, Breyman, Erica, Tosto-Mancuso, Jenna, Dai, Yile, Perotti, Emily, Akduman, Koray, Tzeng, Tiffany J., Xu, Lan, Geraghty, Anna C., Monje, Michelle, Yildirim, Inci, Shon, John, Medzhitov, Ruslan, Lutchmansingh, Denyse, Possick, Jennifer D., Kaminski, Naftali, Omer, Saad B., Krumholz, Harlan M., Guan, Leying, Dela Cruz, Charles S., van Dijk, David, Ring, Aaron M., Putrino, David, Iwasaki, Akiko·2023·Nature

Abstract

Post-acute infection syndromes may develop after acute viral disease 1 . Infection with SARS-CoV-2 can result in the development of a post-acute infection syndrome known as long COVID. Individuals with long COVID frequently report unremitting fatigue, post-exertional malaise, and a variety of cognitive and autonomic dysfunctions 2–4 . However, the biological processes that are associated with the development and persistence of these symptoms are unclear. Here 275 individuals with or without long COVID were enrolled in a cross-sectional study that included multidimensional immune phenotyping and unbiased machine learning methods to identify biological features associated with long COVID. Marked differences were noted in circulating myeloid and lymphocyte populations relative to the matched controls, as well as evidence of exaggerated humoral responses directed against SARS-CoV-2 among participants with long COVID. Furthermore, higher antibody responses directed against non-SARS-CoV-2 viral pathogens were observed among individuals with long COVID, particularly Epstein–Barr virus. Levels of soluble immune mediators and hormones varied among groups, with cortisol levels being lower among participants with long COVID. Integration of immune phenotyping data into unbiased machine learning models identified the key features that are most strongly associated with long COVID status. Collectively, these findings may help to guide future studies into the pathobiology of long COVID and help with developing relevant biomarkers.

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Metadata

Authors
Klein, J., Wood, J., Jaycox, J. R., Dhodapkar, R. M., Lu, P., Gehlhausen, J. R., Tabachnikova, A., Greene, K., Tabacof, L., Malik, A. A., Silva Monteiro, V., Silva, J., Kamath, K., Zhang, M., Dhal, A., Ott, I. M., Valle, G., Peña-Hernández, M., Mao, T., Bhattacharjee, B., Takahashi, T., Lucas, C., Song, E., McCarthy, D., Breyman, E., Tosto-Mancuso, J., Dai, Y., Perotti, E., Akduman, K., Tzeng, T. J., Xu, L., Geraghty, A. C., Monje, M., Yildirim, I., Shon, J., Medzhitov, R., Lutchmansingh, D., Possick, J. D., Kaminski, N., Omer, S. B., Krumholz, H. M., Guan, L., Dela Cruz, C. S., van Dijk, D., Ring, A. M., Putrino, D., & Iwasaki, A.
Venue
Nature
Published
2023-09-25
Volume
623
Issue
7985
Pages
139-148
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W4387012832
Cited by
806
References
28
FWCI
114.40
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Distinguishing features of long COVID identified through immune profiling. https://app.cochat.ai/papers/10.1038/s41586-023-06651-y
The paper
Klein, J., Wood, J., Jaycox, J. R., Dhodapkar, R. M., Lu, P., Gehlhausen, J. R., Tabachnikova, A., Greene, K., Tabacof, L., Malik, A. A., Silva Monteiro, V., Silva, J., Kamath, K., Zhang, M., Dhal, A., Ott, I. M., Valle, G., Peña-Hernández, M., Mao, T., . . . Iwasaki, A. (2023). Distinguishing features of long COVID identified through immune profiling. Nature. https://doi.org/10.1038/s41586-023-06651-y

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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