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CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer.

Research square

Huang A, Bange E, Han N, Wileyto EP, Kim J, Gouma S, Robinson J, Greenplate A, Porterfield F, Owoyemi O, Naik K, Zheng C, Galantino M, Weisman A, Ittner C, Kugler E, Baxter A, Weirick M, McAllister C, Babady NE, Kumar A, Widman A, Dewolf S, Boutemine S, Roberts C, Budzik K, Tollett S, Wright C, Perloff T, Sun L, Mathew D, Giles J, Oldridge D, Wu J, Alanio C, Adamski S, Vella L, Kerr S, Cohen J, Oyer R, Massa R, Maillard I, Maxwell K, Maslak P, Vonderheide R, Wolchok JD, Hensley S, Wherry E, Meyer N, DeMichele A, Vardhana S, Mamtani R, Oniyide O, Agyekum R, Dunn T, Jones T, Giannini H, Garfall A, Reilly J.
PMID: 33564756
Res Sq. 2021 Feb 02; doi: 10.21203/rs.3.rs-162289/v1.

Cancer patients have increased morbidity and mortality from Coronavirus Disease 2019 (COVID-19), but the underlying immune mechanisms are unknown. In a cohort of 100 cancer patients hospitalized for COVID-19 at the University of Pennsylvania Health System, we found that...

Cite
Huang A, Bange E, Han N, et al. CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Res Sq. 2021;doi: 10.21203/rs.3.rs-162289/v1.
Huang, A., Bange, E., Han, N., Wileyto, E. P., Kim, J., Gouma, S., Robinson, J., Greenplate, A., Porterfield, F., Owoyemi, O., Naik, K., Zheng, C., Galantino, M., Weisman, A., Ittner, C., Kugler, E., Baxter, A., Weirick, M., McAllister, C., Babady, N. E., Kumar, A., Widman, A., Dewolf, S., Boutemine, S., Roberts, C., Budzik, K., Tollett, S., Wright, C., Perloff, T., Sun, L., Mathew, D., Giles, J., Oldridge, D., Wu, J., Alanio, C., Adamski, S., Vella, L., Kerr, S., Cohen, J., Oyer, R., Massa, R., Maillard, I., Maxwell, K., Maslak, P., Vonderheide, R., Wolchok, J. D., Hensley, S., Wherry, E., Meyer, N., DeMichele, A., Vardhana, S., Mamtani, R., Oniyide, O., Agyekum, R., Dunn, T., Jones, T., Giannini, H., Garfall, A., & Reilly, J. (2021). CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Research square, . https://doi.org/10.21203/rs.3.rs-162289/v1
Huang, Alexander, et al. "CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer." Research square vol. (2021). doi: https://doi.org/10.21203/rs.3.rs-162289/v1
Huang A, Bange E, Han N, Wileyto EP, Kim J, Gouma S, Robinson J, Greenplate A, Porterfield F, Owoyemi O, Naik K, Zheng C, Galantino M, Weisman A, Ittner C, Kugler E, Baxter A, Weirick M, McAllister C, Babady NE, Kumar A, Widman A, Dewolf S, Boutemine S, Roberts C, Budzik K, Tollett S, Wright C, Perloff T, Sun L, Mathew D, Giles J, Oldridge D, Wu J, Alanio C, Adamski S, Vella L, Kerr S, Cohen J, Oyer R, Massa R, Maillard I, Maxwell K, Maslak P, Vonderheide R, Wolchok JD, Hensley S, Wherry E, Meyer N, DeMichele A, Vardhana S, Mamtani R, Oniyide O, Agyekum R, Dunn T, Jones T, Giannini H, Garfall A, Reilly J. CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Res Sq. 2021 Feb 02; doi: 10.21203/rs.3.rs-162289/v1. PMID: 33564756; PMCID: PMC7872363.
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NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy.

The Journal of experimental medicine

Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM.
PMID: 34882194
J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09.

Pregnancy is a common immunization event, but the molecular mechanisms and immunological consequences provoked by pregnancy remain largely unknown. We used mouse models and human transplant registry data to reveal that pregnancy induced exhausted CD8 T cells (Preg-TEX), which...

Cite
Lewis EL, Xu R, Beltra JC, et al. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2021;219(1)doi: 10.1084/jem.20201599.
Lewis, E. L., Xu, R., Beltra, J. C., Ngiow, S. F., Cohen, J., Telange, R., Crane, A., Sawinski, D., Wherry, E. J., & Porrett, P. M. (2022). NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. The Journal of experimental medicine, 219(1), . https://doi.org/10.1084/jem.20201599
Lewis, Emma L, et al. "NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy." The Journal of experimental medicine vol. 219,1 (2022). doi: https://doi.org/10.1084/jem.20201599
Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09. PMID: 34882194; PMCID: PMC8666877.
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NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy.

The Journal of experimental medicine

Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM.
PMID: 34882194
J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09.

Pregnancy is a common immunization event, but the molecular mechanisms and immunological consequences provoked by pregnancy remain largely unknown. We used mouse models and human transplant registry data to reveal that pregnancy induced exhausted CD8 T cells (Preg-TEX), which...

Cite
Lewis EL, Xu R, Beltra JC, et al. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2021;219(1)doi: 10.1084/jem.20201599.
Lewis, E. L., Xu, R., Beltra, J. C., Ngiow, S. F., Cohen, J., Telange, R., Crane, A., Sawinski, D., Wherry, E. J., & Porrett, P. M. (2022). NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. The Journal of experimental medicine, 219(1), . https://doi.org/10.1084/jem.20201599
Lewis, Emma L, et al. "NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy." The Journal of experimental medicine vol. 219,1 (2022). doi: https://doi.org/10.1084/jem.20201599
Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09. PMID: 34882194; PMCID: PMC8666877.
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Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules.

Nature communications

Vollmann EH, Rattay K, Barreiro O, Thiriot A, Fuhlbrigge RA, Vrbanac V, Kim KW, Jung S, Tager AM, von Andrian UH.
PMID: 34711828
Nat Commun. 2021 Oct 28;12(1):6230. doi: 10.1038/s41467-021-26446-x.

T cells undergo rigorous selection in the thymus to ensure self-tolerance and prevent autoimmunity, with this process requiring innocuous self-antigens (Ags) to be presented to thymocytes. Self-Ags are either expressed by thymic stroma cells or transported to the thymus...

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Vollmann EH, Rattay K, Barreiro O, et al. Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules. Nat Commun. 2021;12(1):6230doi: 10.1038/s41467-021-26446-x.
Vollmann, E. H., Rattay, K., Barreiro, O., Thiriot, A., Fuhlbrigge, R. A., Vrbanac, V., Kim, K. W., Jung, S., Tager, A. M., & von Andrian, U. H. (2021). Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules. Nature communications, 12(1), 6230. https://doi.org/10.1038/s41467-021-26446-x
Vollmann, Elisabeth H, et al. "Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules." Nature communications vol. 12,1 (2021): 6230. doi: https://doi.org/10.1038/s41467-021-26446-x
Vollmann EH, Rattay K, Barreiro O, Thiriot A, Fuhlbrigge RA, Vrbanac V, Kim KW, Jung S, Tager AM, von Andrian UH. Specialized transendothelial dendritic cells mediate thymic T-cell selection against blood-borne macromolecules. Nat Commun. 2021 Oct 28;12(1):6230. doi: 10.1038/s41467-021-26446-x. PMID: 34711828; PMCID: PMC8553756.
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NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy.

The Journal of experimental medicine

Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM.
PMID: 34882194
J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09.

Pregnancy is a common immunization event, but the molecular mechanisms and immunological consequences provoked by pregnancy remain largely unknown. We used mouse models and human transplant registry data to reveal that pregnancy induced exhausted CD8 T cells (Preg-TEX), which...

Cite
Lewis EL, Xu R, Beltra JC, et al. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2021;219(1)doi: 10.1084/jem.20201599.
Lewis, E. L., Xu, R., Beltra, J. C., Ngiow, S. F., Cohen, J., Telange, R., Crane, A., Sawinski, D., Wherry, E. J., & Porrett, P. M. (2022). NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. The Journal of experimental medicine, 219(1), . https://doi.org/10.1084/jem.20201599
Lewis, Emma L, et al. "NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy." The Journal of experimental medicine vol. 219,1 (2022). doi: https://doi.org/10.1084/jem.20201599
Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09. PMID: 34882194; PMCID: PMC8666877.
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Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells.

Science immunology

Herati RS, Muselman A, Vella L, Bengsch B, Parkhouse K, Del Alcazar D, Kotzin J, Doyle SA, Tebas P, Hensley SE, Su LF, Schmader KE, Wherry EJ.
PMID: 28620653
Sci Immunol. 2017 Feb;2(8). doi: 10.1126/sciimmunol.aag2152. Epub 2017 Feb 17.

T follicular helper (Tfh) CD4 cells are crucial providers of B cell help during adaptive immune responses. A circulating population of CD4 T cells, termed cTfh, have similarity to lymphoid Tfh, can provide B cell help, and responded to...

Cite
Herati RS, Muselman A, Vella L, et al. Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells. Sci Immunol. 2017;2(8)doi: 10.1126/sciimmunol.aag2152.
Herati, R. S., Muselman, A., Vella, L., Bengsch, B., Parkhouse, K., Del Alcazar, D., Kotzin, J., Doyle, S. A., Tebas, P., Hensley, S. E., Su, L. F., Schmader, K. E., & Wherry, E. J. (2017). Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells. Science immunology, 2(8), . https://doi.org/10.1126/sciimmunol.aag2152
Herati, Ramin Sedaghat, et al. "Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells." Science immunology vol. 2,8 (2017). doi: https://doi.org/10.1126/sciimmunol.aag2152
Herati RS, Muselman A, Vella L, Bengsch B, Parkhouse K, Del Alcazar D, Kotzin J, Doyle SA, Tebas P, Hensley SE, Su LF, Schmader KE, Wherry EJ. Successive annual influenza vaccination induces a recurrent oligoclonotypic memory response in circulating T follicular helper cells. Sci Immunol. 2017 Feb;2(8). doi: 10.1126/sciimmunol.aag2152. Epub 2017 Feb 17. PMID: 28620653; PMCID: PMC5469419.
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IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease.

JCI insight

Urso K, Alvarez D, Cremasco V, Tsang K, Grauel A, Lafyatis R, von Andrian UH, Ermann J, Aliprantis AO.
PMID: 27547823
JCI Insight. 2016 Aug 04;1(12). doi: 10.1172/jci.insight.88057.

Systemic sclerosis (SSc) is a potentially fatal autoimmune disorder with limited therapeutic options. Sclerodermatous graft versus host disease (sclGvHD), induced by transfer of B10.D2 splenocytes into BALB/c

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Urso K, Alvarez D, Cremasco V, et al. IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease. JCI Insight. 2016;1(12)doi: 10.1172/jci.insight.88057.
Urso, K., Alvarez, D., Cremasco, V., Tsang, K., Grauel, A., Lafyatis, R., von Andrian, U. H., Ermann, J., & Aliprantis, A. O. (2016). IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease. JCI insight, 1(12), . https://doi.org/10.1172/jci.insight.88057
Urso, Katia, et al. "IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease." JCI insight vol. 1,12 (2016). doi: https://doi.org/10.1172/jci.insight.88057
Urso K, Alvarez D, Cremasco V, Tsang K, Grauel A, Lafyatis R, von Andrian UH, Ermann J, Aliprantis AO. IL4RA on lymphatic endothelial cells promotes T cell egress during sclerodermatous graft versus host disease. JCI Insight. 2016 Aug 04;1(12). doi: 10.1172/jci.insight.88057. PMID: 27547823; PMCID: PMC4988402.
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Role of nuclear localization in the regulation and function of T-bet and Eomes in exhausted CD8 T cells.

Cell reports

McLane LM, Ngiow SF, Chen Z, Attanasio J, Manne S, Ruthel G, Wu JE, Staupe RP, Xu W, Amaravadi RK, Xu X, Karakousis GC, Mitchell TC, Schuchter LM, Huang AC, Freedman BD, Betts MR, Wherry EJ.
PMID: 33979613
Cell Rep. 2021 May 11;35(6):109120. doi: 10.1016/j.celrep.2021.109120.

The transcription factors T-bet and Eomesodermin (Eomes) regulate CD8 T cell exhaustion through undefined mechanisms. Here, we show that the subcellular localization of T-bet and Eomes dictate their regulatory activity in exhausted T cells (T

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McLane LM, Ngiow SF, Chen Z, et al. Role of nuclear localization in the regulation and function of T-bet and Eomes in exhausted CD8 T cells. Cell Rep. 2021;35(6):109120doi: 10.1016/j.celrep.2021.109120.
McLane, L. M., Ngiow, S. F., Chen, Z., Attanasio, J., Manne, S., Ruthel, G., Wu, J. E., Staupe, R. P., Xu, W., Amaravadi, R. K., Xu, X., Karakousis, G. C., Mitchell, T. C., Schuchter, L. M., Huang, A. C., Freedman, B. D., Betts, M. R., & Wherry, E. J. (2021). Role of nuclear localization in the regulation and function of T-bet and Eomes in exhausted CD8 T cells. Cell reports, 35(6), 109120. https://doi.org/10.1016/j.celrep.2021.109120
McLane, Laura M, et al. "Role of nuclear localization in the regulation and function of T-bet and Eomes in exhausted CD8 T cells." Cell reports vol. 35,6 (2021): 109120. doi: https://doi.org/10.1016/j.celrep.2021.109120
McLane LM, Ngiow SF, Chen Z, Attanasio J, Manne S, Ruthel G, Wu JE, Staupe RP, Xu W, Amaravadi RK, Xu X, Karakousis GC, Mitchell TC, Schuchter LM, Huang AC, Freedman BD, Betts MR, Wherry EJ. Role of nuclear localization in the regulation and function of T-bet and Eomes in exhausted CD8 T cells. Cell Rep. 2021 May 11;35(6):109120. doi: 10.1016/j.celrep.2021.109120. PMID: 33979613; PMCID: PMC8195461.
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NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy.

The Journal of experimental medicine

Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM.
PMID: 34882194
J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09.

Pregnancy is a common immunization event, but the molecular mechanisms and immunological consequences provoked by pregnancy remain largely unknown. We used mouse models and human transplant registry data to reveal that pregnancy induced exhausted CD8 T cells (Preg-TEX), which...

Cite
Lewis EL, Xu R, Beltra JC, et al. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2021;219(1)doi: 10.1084/jem.20201599.
Lewis, E. L., Xu, R., Beltra, J. C., Ngiow, S. F., Cohen, J., Telange, R., Crane, A., Sawinski, D., Wherry, E. J., & Porrett, P. M. (2022). NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. The Journal of experimental medicine, 219(1), . https://doi.org/10.1084/jem.20201599
Lewis, Emma L, et al. "NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy." The Journal of experimental medicine vol. 219,1 (2022). doi: https://doi.org/10.1084/jem.20201599
Lewis EL, Xu R, Beltra JC, Ngiow SF, Cohen J, Telange R, Crane A, Sawinski D, Wherry EJ, Porrett PM. NFAT-dependent and -independent exhaustion circuits program maternal CD8 T cell hypofunction in pregnancy. J Exp Med. 2022 Jan 03;219(1). doi: 10.1084/jem.20201599. Epub 2021 Dec 09. PMID: 34882194; PMCID: PMC8666877.
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Inhibitory signaling sustains a distinct early memory CD8.

Science immunology

Johnnidis JB, Muroyama Y, Ngiow SF, Chen Z, Manne S, Cai Z, Song S, Platt JM, Schenkel JM, Abdel-Hakeem M, Beltra JC, Greenplate AR, Ali MA, Nzingha K, Giles JR, Harly C, Attanasio J, Pauken KE, Bengsch B, Paley MA, Tomov VT, Kurachi M, Vignali DAA, Sharpe AH, Reiner SL, Bhandoola A, Johnson FB, Wherry EJ.
PMID: 33452106
Sci Immunol. 2021 Jan 15;6(55). doi: 10.1126/sciimmunol.abe3702.

The developmental origins of memory T cells remain incompletely understood. During the expansion phase of acute viral infection, we identified a distinct subset of virus-specific CD8

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Johnnidis JB, Muroyama Y, Ngiow SF, et al. Inhibitory signaling sustains a distinct early memory CD8. Sci Immunol. 2021;6(55)doi: 10.1126/sciimmunol.abe3702.
Johnnidis, J. B., Muroyama, Y., Ngiow, S. F., Chen, Z., Manne, S., Cai, Z., Song, S., Platt, J. M., Schenkel, J. M., Abdel-Hakeem, M., Beltra, J. C., Greenplate, A. R., Ali, M. A., Nzingha, K., Giles, J. R., Harly, C., Attanasio, J., Pauken, K. E., Bengsch, B., Paley, M. A., Tomov, V. T., Kurachi, M., Vignali, D. A. A., Sharpe, A. H., Reiner, S. L., Bhandoola, A., Johnson, F. B., & Wherry, E. J. (2021). Inhibitory signaling sustains a distinct early memory CD8. Science immunology, 6(55), . https://doi.org/10.1126/sciimmunol.abe3702
Johnnidis, Jonathan B, et al. "Inhibitory signaling sustains a distinct early memory CD8." Science immunology vol. 6,55 (2021). doi: https://doi.org/10.1126/sciimmunol.abe3702
Johnnidis JB, Muroyama Y, Ngiow SF, Chen Z, Manne S, Cai Z, Song S, Platt JM, Schenkel JM, Abdel-Hakeem M, Beltra JC, Greenplate AR, Ali MA, Nzingha K, Giles JR, Harly C, Attanasio J, Pauken KE, Bengsch B, Paley MA, Tomov VT, Kurachi M, Vignali DAA, Sharpe AH, Reiner SL, Bhandoola A, Johnson FB, Wherry EJ. Inhibitory signaling sustains a distinct early memory CD8. Sci Immunol. 2021 Jan 15;6(55). doi: 10.1126/sciimmunol.abe3702. PMID: 33452106; PMCID: PMC8258400.
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CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer.

Research square

Huang A, Bange E, Han N, Wileyto EP, Kim J, Gouma S, Robinson J, Greenplate A, Porterfield F, Owoyemi O, Naik K, Zheng C, Galantino M, Weisman A, Ittner C, Kugler E, Baxter A, Weirick M, McAllister C, Babady NE, Kumar A, Widman A, Dewolf S, Boutemine S, Roberts C, Budzik K, Tollett S, Wright C, Perloff T, Sun L, Mathew D, Giles J, Oldridge D, Wu J, Alanio C, Adamski S, Vella L, Kerr S, Cohen J, Oyer R, Massa R, Maillard I, Maxwell K, Maslak P, Vonderheide R, Wolchok JD, Hensley S, Wherry E, Meyer N, DeMichele A, Vardhana S, Mamtani R, Oniyide O, Agyekum R, Dunn T, Jones T, Giannini H, Garfall A, Reilly J.
PMID: 33564756
Res Sq. 2021 Feb 02; doi: 10.21203/rs.3.rs-162289/v1.

Cancer patients have increased morbidity and mortality from Coronavirus Disease 2019 (COVID-19), but the underlying immune mechanisms are unknown. In a cohort of 100 cancer patients hospitalized for COVID-19 at the University of Pennsylvania Health System, we found that...

Cite
Huang A, Bange E, Han N, et al. CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Res Sq. 2021;doi: 10.21203/rs.3.rs-162289/v1.
Huang, A., Bange, E., Han, N., Wileyto, E. P., Kim, J., Gouma, S., Robinson, J., Greenplate, A., Porterfield, F., Owoyemi, O., Naik, K., Zheng, C., Galantino, M., Weisman, A., Ittner, C., Kugler, E., Baxter, A., Weirick, M., McAllister, C., Babady, N. E., Kumar, A., Widman, A., Dewolf, S., Boutemine, S., Roberts, C., Budzik, K., Tollett, S., Wright, C., Perloff, T., Sun, L., Mathew, D., Giles, J., Oldridge, D., Wu, J., Alanio, C., Adamski, S., Vella, L., Kerr, S., Cohen, J., Oyer, R., Massa, R., Maillard, I., Maxwell, K., Maslak, P., Vonderheide, R., Wolchok, J. D., Hensley, S., Wherry, E., Meyer, N., DeMichele, A., Vardhana, S., Mamtani, R., Oniyide, O., Agyekum, R., Dunn, T., Jones, T., Giannini, H., Garfall, A., & Reilly, J. (2021). CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Research square, . https://doi.org/10.21203/rs.3.rs-162289/v1
Huang, Alexander, et al. "CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer." Research square vol. (2021). doi: https://doi.org/10.21203/rs.3.rs-162289/v1
Huang A, Bange E, Han N, Wileyto EP, Kim J, Gouma S, Robinson J, Greenplate A, Porterfield F, Owoyemi O, Naik K, Zheng C, Galantino M, Weisman A, Ittner C, Kugler E, Baxter A, Weirick M, McAllister C, Babady NE, Kumar A, Widman A, Dewolf S, Boutemine S, Roberts C, Budzik K, Tollett S, Wright C, Perloff T, Sun L, Mathew D, Giles J, Oldridge D, Wu J, Alanio C, Adamski S, Vella L, Kerr S, Cohen J, Oyer R, Massa R, Maillard I, Maxwell K, Maslak P, Vonderheide R, Wolchok JD, Hensley S, Wherry E, Meyer N, DeMichele A, Vardhana S, Mamtani R, Oniyide O, Agyekum R, Dunn T, Jones T, Giannini H, Garfall A, Reilly J. CD8 T cells compensate for impaired humoral immunity in COVID-19 patients with hematologic cancer. Res Sq. 2021 Feb 02; doi: 10.21203/rs.3.rs-162289/v1. PMID: 33564756; PMCID: PMC7872363.
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