Distinguishing Incubation and Acute Disease Stages of Mild-to-Moderate COVID-19

被引:2
作者
Mueller, Michael [1 ]
Volzke, Johann [1 ]
Subin, Behnam [2 ]
Schmidt, Christian Johann [1 ]
Geerdes-Fenge, Hilte [3 ]
Reisinger, Emil Christian [3 ]
Mueller-Hilke, Brigitte [1 ]
机构
[1] Rostock Univ, Med Ctr, Core Facil Cell Sorting & Cell Anal, D-18057 Rostock, Germany
[2] Rostock Univ, Med Ctr, Dept Cardiol, D-18057 Rostock, Germany
[3] Rostock Univ, Med Ctr, Dept Trop Med & Infect Dis, D-18057 Rostock, Germany
来源
VIRUSES-BASEL | 2022年 / 14卷 / 02期
关键词
SARS-CoV-2; COVID-19; disease phases; plasmablasts; cytotoxic T cells; IP-10; acute infection; antibodies; HUMAN-IMMUNODEFICIENCY-VIRUS; INFECTION; CELLS; EXPANSION;
D O I
10.3390/v14020203
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
While numerous studies have already compared the immune responses against SARS-CoV-2 in severely and mild-to-moderately ill COVID-19 patients, longitudinal trajectories are still scarce. We therefore set out to analyze serial blood samples from mild-to-moderately ill patients in order to define the immune landscapes for differently progressed disease stages. Twenty-two COVID-19 patients were subjected to consecutive venipuncture within seven days after diagnosis or admittance to hospital. Flow cytometry was performed to analyze peripheral blood immune cell compositions and their activation as were plasma levels of cytokines and SARS-CoV-2 specific immunoglobulins. Healthy donors served as controls. Integrating the kinetics of plasmablasts and SARS-CoV-2 specific antibodies allowed for the definition of three disease stages of early COVID-19. The incubation phase was characterized by a sharp increase in pro-inflammatory monocytes and terminally differentiated cytotoxic T cells. The latter correlated significantly with elevated concentrations of IP-10. Early acute infection featured a peak in PD-1(+) cytotoxic T cells, plasmablasts and increasing titers of virus specific antibodies. During late acute infection, immature neutrophils were enriched, whereas all other parameters returned to baseline. Our findings will help to define landmarks that are indispensable for the refinement of new anti-viral and anti-inflammatory therapeutics, and may also inform clinicians to optimize treatment and prevent fatal outcomes.
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页数:17
相关论文
共 40 条
[11]   VIRUS BURDEN IN LONG-TERM SURVIVORS OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) INFECTION IS A DETERMINANT OF ANTI-HIV CD8(+) LYMPHOCYTE ACTIVITY [J].
FERBAS, J ;
KAPLAN, AH ;
HAUSNER, MA ;
HULTIN, LE ;
MATUD, JL ;
LIU, ZY ;
PANICALI, DL ;
NERNGHO, H ;
DETELS, R ;
GIORGI, JV .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (02) :329-339
[12]   Monocyte-Plasmablast Crosstalk during Dengue [J].
Green, Angela M. ;
Harris, Eva .
CELL HOST & MICROBE, 2014, 16 (01) :7-9
[13]   Profiling Early Humoral Response to Diagnose Novel Coronavirus Disease (COVID-19) [J].
Guo, Li ;
Ren, Lili ;
Yang, Siyuan ;
Xiao, Meng ;
Chang, De ;
Yang, Fan ;
Dela Cruz, Charles S. ;
Wang, Yingying ;
Wu, Chao ;
Xiao, Yan ;
Zhang, Lulu ;
Han, Lianlian ;
Dang, Shengyuan ;
Xu, Yan ;
Yang, Qi-Wen ;
Xu, Sheng-Yong ;
Zhu, Hua-Dong ;
Xu, Ying-Chun ;
Jin, Qi ;
Sharma, Lokesh ;
Wang, Linghang ;
Wang, Jianwei .
CLINICAL INFECTIOUS DISEASES, 2020, 71 (15) :778-785
[14]   SARS-CoV-2 infection rates of antibody-positive compared with antibody-negative health-care workers in England: a large, multicentre, prospective cohort study (SIREN) [J].
Hall, Victoria Jane ;
Foulkes, Sarah ;
Charlett, Andre ;
Atti, Ana ;
Monk, Edward J. M. ;
Simmons, Ruth ;
Wellington, Edgar ;
Cole, Michelle J. ;
Saei, Ayoub ;
Oguti, Blanche ;
Munro, Katie ;
Wallace, Sarah ;
Kirwan, Peter D. ;
Shrotri, Madhumita ;
Vusirikala, Amoolya ;
Rokadiya, Sakib ;
Kall, Meaghan ;
Zambon, Maria ;
Ramsay, Mary ;
Brooks, Tim ;
Brown, Colin S. ;
Chand, Meera A. ;
Hopkins, Susan .
LANCET, 2021, 397 (10283) :1459-1469
[15]  
HAMPL H, 1995, MED MICROBIOL IMMUN, V184, P69
[16]   Neutrophils and COVID-19: Active Participants and Rational Therapeutic Targets [J].
Hazeldine, Jon ;
Lord, Janet M. .
FRONTIERS IN IMMUNOLOGY, 2021, 12
[17]   A diamidobenzimidazole STING agonist protects against SARS-CoV-2 infection [J].
Humphries, Fiachra ;
Shmuel-Galia, Liraz ;
Jiang, Zhaozhao ;
Wilson, Ruth ;
Landis, Philip ;
Ng, Sze-Ling ;
Parsi, Krishna-Mohan ;
Maehr, Rene ;
Cruz, John ;
Morales-Ramos, Angel ;
Ramanjulu, Joshi M. ;
Bertin, John ;
Pesiridis, G. Scott ;
Fitzgerald, Katherine A. .
SCIENCE IMMUNOLOGY, 2021, 6 (59)
[18]   Baseline T-lymphocyte subset absolute counts can predict both outcome and severity in SARS-CoV-2 infected patients: a single center study [J].
Iannetta, Marco ;
Buccisano, Francesco ;
Fraboni, Daniela ;
Malagnino, Vincenzo ;
Campogiani, Laura ;
Teti, Elisabetta ;
Spalliera, Ilaria ;
Rossi, Benedetta ;
Di Lorenzo, Andrea ;
Palmieri, Raffaele ;
Crea, Angela ;
Zordan, Marta ;
Vitale, Pietro ;
Voso, Maria Teresa ;
Andreoni, Massimo ;
Sarmati, Loredana .
SCIENTIFIC REPORTS, 2021, 11 (01)
[19]   Evolution and Diversity of Immune Responses during Acute HIV Infection [J].
Kazer, Samuel W. ;
Walker, Bruce D. ;
Shalek, Alex K. .
IMMUNITY, 2020, 53 (05) :908-924
[20]   SARS-CoV-2 Variants and Vaccines [J].
Krause, Philip R. ;
Fleming, Thomas R. ;
Longini, Ira M. ;
Peto, Richard ;
Briand, Sylvie ;
Heymann, David L. ;
Beral, Valerie ;
Snape, Matthew D. ;
Rees, Helen ;
Ropero, Alba-Maria ;
Balicer, Ran D. ;
Cramer, Jakob P. ;
Munoz-Fontela, Cesar ;
Gruber, Marion ;
Gaspar, Rogerio ;
Singh, Jerome A. ;
Subbarao, Kanta ;
Van Kerkhove, Maria D. ;
Swaminathan, Soumya ;
Ryan, Michael J. ;
Henao-Restrepo, Ana-Maria .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (02) :179-186