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. Author manuscript; available in PMC: 2021 Dec 8.
Published in final edited form as: Am J Transplant. 2021 Sep 30;22(2):669–672. doi: 10.1111/ajt.16841

Table 1.

Demographics and Clinical Characteristics of Study Participants Who Provided an Antibody Titer One Month After Vaccine 2, Stratified by Humoral Response

n (%) Positive Response After
Vaccine 2
(n = 33)a
Negative Response After Vaccine 2
(n = 12)a
P-Valueb

Demographics
 Age Group, years 1.0
  12–15 28 (84.9) 11 (91.7)
  16+ 5 (15.2) 1 (8.3)
 Sex, male 14 (42.4) 5 (41.7) 1.0
 Race, whitec 22 (71) 9 (90) 0.4
 Hispanic or Latino, yesd 2 (6.3) 0 (0) 1.0
Transplant Characteristics
 Organ 0.068
  Liver 17 (51.5) 2 (16.7)
  Kidney 8 (24.2) 5 (41.7)
  Heart 8 (24.2) 4 (33.3)
  Liver-Kidney 0 (0) 1 (8.3)
 Time Since Transplant, years 0.024
  <3 2 (6.1) 5 (41.7)
  3–11 18 (54.6) 4 (33.3)
  ≥12 13 (39.4) 3 (25)
 <3 vs ≥3 Years Since Transplant 0.010
Immunosuppression Regimen
 Number of Agentse 0.013
  0 1 (3.1) 1 (10)
  1 15 (46.9) 0 (0)
  2 10 (31.3) 4 (40)
  3+ 6 (18.8) 5 (50)
 Single vs Multiple Agents (2+)e 0.031
 Agents Usedf
  Tacrolimusg 29 (87.9) 10 (90.9) 1.0
  Anti-metaboliteh 14 (42.4) 10 (83.3) 0.020
  Sirolimusi 6 (18.8) 1 (10) 1.0
  Corticosteroids 5 (15.2) 5 (41.7) 0.10
  Cyclosporine 3 (9.1) 0 (0) 0.6
Treated for Rejection in Past 6 Monthsj,k 1 (3.3) 1 (10) 0.4
a

Table includes any patient in the study who had an antibody result available one month after their second vaccine, regardless of whether the patient was positive or negative after their first vaccine. Table does not include patients who reported a prior history of COVID, history of a pre-vaccination positive SARS-CoV-2 antibody test, or positive baseline serology in our study.

b

All univariate statistical comparisons were performed using the Fisher’s exact test.

c

4 missing (2 positive, 2 negative)

d

3 missing (1 positive, 2 negative)

e

3 patients excluded because of incomplete data

f

Includes reported immunosuppression agents used at start of the study or at time of vaccine 1. Immunosuppression was not mutually exclusive, as some patients were on multiple agents. 0 patients were on everolimus or belatacept for their baseline immunosuppresion regimen prior to this study. 0 patients reported being on medications for other immune conditions including adalimumab, anakinra, baricitinib, belimumab, budesonide, certolizumab, cyclophosphamide, etanercept, hydroxychloroquine, infliximab, leflunomide, methotrexate, natalizumab, ocrelizumab, rituximab, sulfasalazine, tocilizumab, tofacitinib, and ustekinumab.

g

1 missing (negative)

h

Includes myophenolate mofetil, mycophenolic acid, or azathioprine

i

3 missing (1 positive, 2 negative)

j

5 missing (3 positive, 2 negative)

k

No patients received rituximab, IVIG, plasma exchange, or thymoglobulin in the 6 months prior to this study.