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Rapid clinical recovery of a SARS-CoV-2 infected common variable immunodeficiency patient following the infusion of COVID-19 convalescent plasma



Common variable immunodeficiency is the most prevalent symptomatic primary immunodeficiency in adults. Affected patients fail to mount an appropriate humoral response against community acquired infectious diseases and recent reports have provided data supporting the increased susceptibility of these patients to severe SARS-CoV-2 infections. In this context, the infusion of COVID-19 convalescent plasma could represent an effective therapeutic strategy.

Case presentation

25-year old woman diagnosed with common variable immunodeficiency in 2013, developed severe COVID-19 that rapidly progressed to pneumonia presenting with multiple bilateral lung opacities that were both central and peripheral and presented as ground-glass and consolidation types involving all lobes, bilaterally. As blood oxygen saturation decayed and lung abnormalities were not responsive to large spectrum antibiotics and corticosteroids, patient was placed on mechanical ventilation and compassionate-use of approved COVID-19 convalescent donor plasma was introduced. The patient presented a rapid response to the approach and mechanical ventilation could be interrupted 24 h after first dose of COVID-19 convalescent donor plasma. As a whole, the patient received four doses of 200 mL convalescent plasma during a period of 6 days. There was rapid improvement of clinical status, with interruption of supplemental oxygen therapy after 6 days and reduction of lung abnormalities as evidence by sequential computed tomography scans.


This is a single patient report that adds to other few reports on common variable immunodeficiency and agammaglobulinemia, suggesting that COVID-19 convalescent donor plasma could be a valuable therapeutic approach to treat patients affected by dysgammaglobulinemias and presenting severe COVID-19.


Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immunodeficiency affecting adults [1,2,3]. It is characterized by hypogammaglobulinemia, failure to produce specific antibodies and susceptibility to infections [1,2,3]. Affected patients present poor response to vaccines and defective capacity to mount an adaptive response to pathogens, including viruses [4]. As a rule, CVID patients are treated with immunoglobulin replacement, which promotes efficient protection against most community acquired infectious diseases [2]. The effectiveness of immunoglobulin replacement relies on the fact that commercially available human immunoglobulins are produced from pools of donors, warranting a wide spectrum of antibody diversity. Unfortunately, the recent emergence of COVID-19 could represent a particular risk for CVID patients because currently available immunoglobulins were produced from blood samples donated before, or in the early stages of COVID-19 pandemics, implying that most donors might not have been immunized against SARS-CoV-2. In addition, a recent study has reported that human adaptive memory to coronaviruses is short-lasting, which may suggest that even in the future, the presence of immunoneutralizing antibodies against SARS-CoV-2 in donor immunoglobulin could be scarce [5]. Recent reports have provided insights and data to support the increased susceptibility of CVID and also agammaglobulinemia patients to severe SARS-CoV-2 infections [6,7,8,9]. In this context, it has been proposed that infusion of COVID-19 convalescent plasma could represent an effective approach to treat CVID patients developing COVID-19 [10].

Case presentation

Here, we report the case of a 25-year old woman diagnosed with CVID in 2013 that was infected with SARS-CoV-2 developing severe COVID-19 and presenting rapid response to COVID-19 convalescent plasma infusion. Except for CVID, the patient had no other comorbidity, had no family records for any primary immunodeficiency, was lean and practiced sports frequently. At the time of CVID diagnosis that was defined on the basis of the recommendations of the International Consensus Document (ICON): Common Variable Immunodeficiency Disorders [3], patient reported recurrent infections of the upper respiratory tract and lungs, beginning in 2000 (at the age of 5-y); blood IgG was 0.071 g/L (normal range 5.4–16.1 g/L); IgA was 0.22 g/L (normal range 0.80–2.80 g/L); and, peripheral blood cell immunophenotyping determined 86% CD3, 52% CD4, 31% CD8, 4.1% CD19 and 6.2% CD16 + CD56. In addition, she presented absent baseline and post-vaccinal humoral response to pathogen-derived peptide and polysaccharide antigens. Immunoglobulin replacement was introduced in 2013 and administered regularly without interruptions thenceforth. The initial dose was 400 mg/kg every 28 days and after adjustments based on the stabilization of blood IgG at minimum 8.0 g/L, maintenance dose was defined as 25 g every 28 days (345 mg/kg/dose). From 2013 to 2020, patient was constantly monitored in regular visits to the University of Campinas Clinics Hospital. She was regularly submitted to blood IgG determinations and clinically evaluated for signs of uncontrolled disease, such as infections, autoimmunity, inflammatory conditions and neoplasia. During the entire period, treatment was efficient to keep her on optimal medical condition. The determinations of blood IgG in the months prior to SARS-CoV-2 infection confirmed the effectiveness of the treatment (IgG = 10.04 g/L in November 2019; IgG = 10.01 g/L in July 2020). Lung CT scan at CVID diagnosis (2013) revealed sparse areas of fibrosis and bronchiectasis predominantly in the anterior and superior segments of the right lung inferior lobe; inferior and superior lingular segments of left lung superior lobe and anterior portions of the left lung inferior lobe (Fig. 1a). During follow up, from 2013 to 2020, no additional lung CT scans were performed because patient presented an optimal response to therapeutic intervention.

Fig. 1

Lung computed tomography scans obtained at the time of common variable immunodeficiency diagnosis, in 2013 (a) and during COVID-19, (be). The dates when scans were performed are depicted in the Figure. As for the interpretation of scans, the patient was submitted to a breast implant in 2017

On August 8, 2020, the patient was admitted at her hometown Hospital with fever (39.8 °C), cough, dyspnea and 95% blood O2 saturation. Lung CT scan (Fig. 1b) revealed multiple bilateral lung opacities that were both central and peripheral and presented as ground-glass and consolidation types involving all lobes, bilaterally, suggesting COVID-19 and scoring 9 according to the COVID-19 lung CT scoring system published elsewhere [11]. Despite clinical and radiological evidence for COVID-19, the real-time PCR from a nasopharynx sample was negative for SARS-CoV-2. The patient was administered low-flow supplemental oxygen and treated with antibiotics and corticosteroid. As fever continued, lung CT scan score progressed to 14 (Fig. 1c) and dyspnea progressively worsened, supplemental oxygen was increased to high-flow and on August 13, the patient was transferred to the high-complexity University of Campinas Clinics Hospital. On admittance, a new nasopharyngeal swab was collected, which scored positive for SARS-CoV-2 on real-time PCR. At this stage, blood O2 saturation was 91% on ambient air and patient was maintained on high-flux supplemental oxygen. A wider spectrum antibiotic was introduced, and dexamethasone was administered in a dose previously shown to be most effective for severe COVID-19 [12]. Blood O2 saturation was continuously monitored and supplemental O2 was adjusted accordingly. Despite intense clinical and pharmacological therapy, fever and dyspnea persisted and on August 17, blood O2 saturation was 85% on high-flux supplemental oxygen. A new lung CT scan revealed considerable worsening of the lung damage, scoring 22 (Fig. 1d). The patient was transferred to the intensive care unit and placed on invasive mechanical ventilation. At this stage, total blood IgG was 6.08 g/L, and both sputum and blood cultures were negative for bacterial and fungal infections. On August 19, as no clinical improvement was obtained, we decided for compassionate-use approved COVID-19 convalescent donor plasma (200 mL, 1/1280 SARS-Cov-2 specific neutralizing antibody (nAb) plus 200 mL, 1/320 nAb). The patient’s blood levels of anti-SARS-CoV-2 IgM and IgG antibodies scored negative using two distinct tests (OnSite Beijing Genesee Biotech, Inc., China and Architect Abbott, Ireland) [13].

Each convalescent plasma unit was obtained from a different donor by apheresis using the Amicus™ automated blood cell separator (Fresenius Kabi AG, Bad Homburg, Germany). Donation criteria included: laboratory confirmation of previous SARS-Cov-2 infection through positive RT-PCR test result, absence of symptoms for at least 28 days and eligibility for other clinical and laboratory blood donation criteria in accordance with national legislation. The evaluation of SARS-Cov-2 specific nAb titers was performed by observing the cytopathic effect in cultures of Vero cells incubated with a serum-virus mixture. After 3 days of incubation, Vero cells were inspected by an inverted optical microscope; the highest serum dilution that protected more than 80% of cells from cytopathic effect was taken as the neutralization titer. These procedures were carried out within a clinical trial approved by the Brazilian Commission on Ethics on Research (CONEP, Approval number 4.021.484).

On August 20, the patient presented improvement of respiratory condition with blood O2 saturation 100% on mechanical ventilation and placed on progressive reduction of FiO2. As fever ceased and cardiovascular and respiratory conditions were stable, mechanical ventilation was interrupted and the patient was returned to high-flow oxygen supplementation. On August 21, blood O2 saturation was 96% and supplemental oxygen was reduced to low-flow. Patient presented no fever and an additional dose of COVID-19 convalescent donor plasma (200 mL, 1/320 nAb) was administered. On August 22, patient was stable, with no fever and a new lung-CT scan revealed remarkable improvement scoring 11 (Fig. 1e). On August 24, a final dose of COVID-19 convalescent donor plasma (200 mL, 1/320 nAb) was administered; patient was removed from supplemental oxygen and blood O2 saturation was 97%. On August 26, patient was discharged presenting blood O2 saturation 94% on ambient air. Anti-SARS-CoV-2 IgM antibodies scored positive, whereas IgG scored borderline. As for September 21, patient was asymptomatic and free from SARS-CoV-2 infection.

Discussion and conclusions

This is a single patient report that adds to other few reports on CVID and agammaglobulinemia, suggesting that COVID-19 convalescent donor plasma could be a valuable therapeutic approach to treat patients affected by dysgammaglobulinemias and presenting severe COVID-19 [6,7,8,9,10, 14]. Further studies, with larger cohorts should be performed to determine the detailed therapeutic outcomes of COVID-19 convalescent donor plasma in patients with abnormal capacity to produce antibody responses.

Availability of data and materials

Does not apply.



Coronavirus diseases-2019


Computed tomography


Common variable immunodeficiency


International Consensus Document: Common Variable Immunodeficiency Disorders


Neutralizing antibodies


  1. 1.

    Gereige JD, Maglione PJ. Current understanding and recent developments in common variable immunodeficiency associated autoimmunity. Front Immunol. 2019;10:2753.

    CAS  Article  Google Scholar 

  2. 2.

    Abolhassani H, Sagvand BT, Shokuhfar T, Mirminachi B, Rezaei N, Aghamohammadi A. A review on guidelines for management and treatment of common variable immunodeficiency. Expert Rev Clin Immunol. 2013;9(6):561–74 (quiz 75).

    CAS  Article  Google Scholar 

  3. 3.

    Bonilla FA, Barlan I, Chapel H, Costa-Carvalho BT, Cunningham-Rundles C, de la Morena MT, et al. International Consensus Document (ICON): common variable immunodeficiency disorders. J Allergy Clin Immunol Pract. 2016;4(1):38–59.

    Article  Google Scholar 

  4. 4.

    Burton DR. Antibodies, viruses and vaccines. Nat Rev Immunol. 2002;2(9):706–13.

    CAS  Article  Google Scholar 

  5. 5.

    Liu STH, Lin HM, Baine I, Wajnberg A, Gumprecht JP, Rahman F, et al. Convalescent plasma treatment of severe COVID-19: a propensity score-matched control study. Nat Med 2020 26(11):1708–13

    Article  Google Scholar 

  6. 6.

    Pulvirenti F, Cinetto F, Milito C, Bonanni L, Pesce AM, Leodori G, et al. Health-related quality of life in common variable immunodeficiency Italian patients switched to remote assistance during the COVID-19 pandemic. J Allergy Clin Immunol Pract. 2020;8(6):1894-9.e2.

    Article  Google Scholar 

  7. 7.

    Quinti I, Lougaris V, Milito C, Cinetto F, Pecoraro A, Mezzaroma I, et al. A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia. J Allergy Clin Immunol. 2020;146(1):211-3.e4.

    CAS  Article  Google Scholar 

  8. 8.

    Fill L, Hadney L, Graven K, Persaud R, Hostoffer R. The clinical observation of a patient with common variable immunodeficiency diagnosed as having coronavirus disease 2019. Ann Allergy Asthma Immunol. 2020;125(1):112–4.

    CAS  Article  Google Scholar 

  9. 9.

    Soresina A, Moratto D, Chiarini M, Paolillo C, Baresi G, Foca E, et al. Two X-linked agammaglobulinemia patients develop pneumonia as COVID-19 manifestation but recover. Pediatr Allergy Immunol. 2020;31(5):565–9.

    Article  Google Scholar 

  10. 10.

    Mira E, Yarce OA, Ortega C, Fernandez S, Pascual NM, Gomez C, et al. Rapid recovery of a SARS-CoV-2-infected X-linked agammaglobulinemia patient after infusion of COVID-19 convalescent plasma. J Allergy Clin Immunol Pract. 2020;8(8):2793–5.

    Article  Google Scholar 

  11. 11.

    Pan F, Ye T, Sun P, Gui S, Liang B, Li L, et al. Time course of lung changes at chest CT during recovery from coronavirus disease 2019 (COVID-19). Radiology. 2020;295(3):715–21.

    Article  Google Scholar 

  12. 12.

    Group RC, Horby P, Lim WS, Emberson JR, Mafham M, Bell JL, et al. Dexamethasone in hospitalized patients with Covid-19—preliminary report. N Engl J Med. 2020.

    Article  Google Scholar 

  13. 13.

    Bryan A, Pepper G, Wener MH, Fink SL, Morishima C, Chaudhary A, et al. Performance characteristics of the abbott architect SARS-CoV-2 IgG assay and seroprevalence in Boise, Idaho. J Clin Microbiol. 2020;58(8):e00941.

    CAS  Article  Google Scholar 

  14. 14.

    Jin H, Reed JC, Liu STH, Ho HE, Lopes JP, Ramsey NB, et al. Three patients with X-linked agammaglobulinemia hospitalized for COVID-19 improved with convalescent plasma. J Allergy Clin Immunol Prac 2020;8(10):3594–3596.e3.

    Article  PubMed  PubMed Central  Google Scholar 

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We thank Professor Sara Saad for her leading role organizing the hematology team for engaging into convalescent plasma production.


LAV is supported by Grants from Sao Paulo Research Foundation (FAPESP #2013/07607-8 and #2020/04522-5), BDB is supported by Grant from the National Council for Scientific and Technological Development (CNPq, #401977/2020), JLPM is supported by Grants from FAPESP (#2016/00194-8 and 2020/04558-0) and STOS is supported by the University Fund for Support to Research (FAEPEX #519292).

Author information




LCR, RGU, TAN, EM, RLZ and LAV were the clinical team that treated the patient during her stay at the hospital. BDB, CC-L, MA-C, JLP-M, FG, VAdC, AdSSD, ABZ and ECA, prepared and/or conducted the intervention with COVID-19 convalescent plasma. LAV prepared the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Licio A. Velloso.

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The study was approved by the Brazilian Commission on Ethics on Research (CONEP, Approval number 4.021.484) and the term of consent to participate was signed by the mother of the patient.

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All authors have provided consent for publication of these data.

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The authors have no competing interests to declare.

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Ribeiro, L.C., Benites, B.D., Ulaf, R.G. et al. Rapid clinical recovery of a SARS-CoV-2 infected common variable immunodeficiency patient following the infusion of COVID-19 convalescent plasma. Allergy Asthma Clin Immunol 17, 14 (2021).

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  • Hypogammaglobulinemia
  • B-lymphocyte
  • Infection
  • Pneumonia
  • Lung
  • Computed tomography