Literature DB >> 33887315

Low immunization rates among kidney transplant recipients who received 2 doses of the mRNA-1273 SARS-CoV-2 vaccine.

Ilies Benotmane1, Gabriela Gautier-Vargas2, Noëlle Cognard2, Jérôme Olagne2, Françoise Heibel2, Laura Braun-Parvez2, Jonas Martzloff2, Peggy Perrin2, Bruno Moulin3, Samira Fafi-Kremer4, Sophie Caillard3.   

Abstract

Entities:  

Year:  2021        PMID: 33887315      PMCID: PMC8055921          DOI: 10.1016/j.kint.2021.04.005

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


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To the editor: The efficacy rates of vaccines to prevent infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have not been specifically investigated in kidney transplant recipient (KTRs). Preliminary results suggest that among KTRs who received the first injection of an mRNA-based vaccine, the antibody response is weak. , This study reports on the immunization rates of KTRs who received 2 doses of the mRNA-1273 SARS-CoV-2 vaccine (Moderna). All participants had a negative history for coronavirus disease 2019 (COVID-19) and tested negative for anti–SARS-CoV-2 antibodies on the day of first injection. Serologic response was assessed on the day of the second injection and 1 month thereafter using the ARCHITECT IgG II Quant test (Abbott). Titers >50 arbitrary units (AUs)/ml were considered positive (detection range, 6.8–80,000 AUs/ml). This assay is reported to correlate with in vitro virus neutralization. The study sample consisted of 205 KTRs (Table 1 ). Only 98 patients displayed a positive serology 28 days after the second dose. The median antibody titer was 803.2 AUs/ml (interquartile range, 142.6−4609.6 AUs/ml). Compared with patients who did not respond after the first injection, patients with a positive serology after the first dose (n = 24 [11.7%]) displayed a higher antibody titer after the second injection (104 vs. 9415 AUs/ml, respectively; P = 7.3–11). Antibody titers measured 1 month after the first and second injections were significantly correlated to each other (Figure 1 a). Patients with a first kidney transplantation, a longer time from transplantation, better kidney function, and less immunosuppression were more likely to seroconvert (Table 1). Patients treated with calcineurin inhibitors, mycophenolate mofetil, or steroids showed significantly lower anti–SARS-CoV-2 antibody titers (Figure 1b–f). One patient developed a severe form of COVID-19 five days after the second injection.
Table 1

Characteristics of kidney transplant recipients stratified according to the serologic response after 2 doses of the mRNA-1273 SARS-CoV-2 vaccine

CharacteristicsEntire cohort (n = 204)aSARS-CoV-2–seronegative patients (n = 106)SARS-CoV-2–seropositive patients (n = 98)PMissing data
Age, yr57.7 (49.4–67.5)58 (51–67.7)57.3 (46.9–66.2)0.450
Male sex130 (63.8)66 (62.3)64 (65.3)0.660
BMI, kg/m225.6 (22.4–28.5)25.4 (22.3–27.6)25.9 (22.6–29.9)0.32
Time from kidney transplantation, yr6.2 (3–12.8)5.4 (2.4–12)7.1 (3.8–14.7)0.041
First transplantation170 (83.3)80 (75.5)90 (91.8)0.0020
Deceased donor163 (79.9)84 (79.3)79 (80.6)0.860
ABO group0.12
 O84 (41.6)38 (36.5)46 (46.9)
 A86 (42.6)48 (46.2)38 (38.8)
 B11 (10.9)15 (14.4)7 (7.1)
 AB10 (5)3 (2.9)7 (7.1)
Induction treatment0.59
 Anti-thymocyte globulin118 (60.5)63 (61.8)55 (59.1)
 Anti-CD2570 (35.9)37 (36.3)33 (35.5)
 No induction7 (3.6)2 (2)5 (5.4)
CNI0.130
Tacrolimus115 (56.4)67 (63.2)48 (49)
Cyclosporine73 (35.8)32 (30.2)41 (41.8)
No CNI16 (7.8)7 (6.6)9 (9.2)
MMF/MPA161 (78.9)91 (85.9)70 (71.4)0.020
Azathioprine6 (2.9)06 (6.12)0.010
mTOR inhibitors27 (13.2)9 (8.5)18 (18.4)0.040
Steroids122 (59.8)69 (65.1)53 (54.1)0.120
Tacrolimus + MMF/MPA98 (48)60 (56.6)38 (38.8)0.0010
Tacrolimus + MMF/MPA + steroids64 (31.3)46 (43.4)18 (18.4)0.00010
Belatacept5 (2.5)4 (3.8)1 (1)0.370
eGFR, ml/min per 1.73 m257.1 (42.4–70.6)54.4 (38.1–67.5)62.5 (47.8–72.5)0.0041
Serum creatinine, μmol/L120 (100–161)137 (109–173)110 (96–141)0.00031

BMI, body mass index; CNI, calcineurin inhibitor; COVID-19, coronavirus disease 2019; eGFR, estimated glomerular filtration rate; MMF, mycophenolate mofetil; MPA, mycophenolic acid; mTOR, mammalian target of rapamycin; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Continuous variables are presented as medians (interquartile ranges), whereas categorical variables are given as n (%).

The patient who developed COVID-19 was excluded from the analysis.

Figure 1

Anti-spike IgG antibody titers (arbitrary unit [AU]/ml) measured after the second injection of the mRNA-1273 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in 204 kidney transplant recipients without a history of coronavirus disease 2019 (COVID-19). Patients with titers >50 AU/ml were considered as seropositive. Bars represent median values. (a) Scattergram showing a significant positive correlation between anti-spike IgG antibody titers (AU/ml) after the first and second vaccine injections (Spearman ρ = 0.68; P < 0.0001). (b) Kidney transplant recipients being treated with antimetabolites (mycophenolate mofetil [MMF]/mycophenolic acid [MPA]) had lower median antibody titers compared with those who did not receive antimetabolites (21.2 [interquartile range {IQR}, 6.8−401.9] AU/ml vs. 147.4 [IQR, 27.5−3352.5] AU/ml, respectively; P = 0.0005). (c) Kidney transplant recipients being treated with steroids had lower median antibody titers compared with those who did not receive steroids (17.9 [IQR, 6.8−378.9] AU/ml vs. 74.8 [IQR, 7.2−2417.9] AU/ml; P = 0.002). (d) Kidney transplant recipients being treated with calcineurin inhibitors (CNIs) had lower median antibody titers compared with those who did not receive CNIs (18.1 [IQR, 6.8−330] AU/ml for patients under tacrolimus and 76.6 [IQR, 10.1−2392.2] AU/ml for patients under cyclosporine vs. 220 [IQR, 6.8−4269] AU/ml for patients who did not receive CNIs). (e) Kidney transplant recipients being treated with tacrolimus + antimetabolites (MMF/MPA) had lower median antibody titers compared with those did not (9.2 [IQR, 6.8−110.2] AU/ml vs. 90.9 [IQR, 7.7−1976] AU/ml, respectively; P < 0.0001). (f) Kidney transplant recipients being treated with tacrolimus + antimetabolites (MMF/MPA) + steroids had lower median antibody titers compared with those who did not (6.8 [IQR, 6.8−57.4] AU/ml vs. 79.4 [IQR, 6.9−1393.5] AU/ml, respectively; P < 0.0001).

Characteristics of kidney transplant recipients stratified according to the serologic response after 2 doses of the mRNA-1273 SARS-CoV-2 vaccine BMI, body mass index; CNI, calcineurin inhibitor; COVID-19, coronavirus disease 2019; eGFR, estimated glomerular filtration rate; MMF, mycophenolate mofetil; MPA, mycophenolic acid; mTOR, mammalian target of rapamycin; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2. Continuous variables are presented as medians (interquartile ranges), whereas categorical variables are given as n (%). The patient who developed COVID-19 was excluded from the analysis. Anti-spike IgG antibody titers (arbitrary unit [AU]/ml) measured after the second injection of the mRNA-1273 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in 204 kidney transplant recipients without a history of coronavirus disease 2019 (COVID-19). Patients with titers >50 AU/ml were considered as seropositive. Bars represent median values. (a) Scattergram showing a significant positive correlation between anti-spike IgG antibody titers (AU/ml) after the first and second vaccine injections (Spearman ρ = 0.68; P < 0.0001). (b) Kidney transplant recipients being treated with antimetabolites (mycophenolate mofetil [MMF]/mycophenolic acid [MPA]) had lower median antibody titers compared with those who did not receive antimetabolites (21.2 [interquartile range {IQR}, 6.8−401.9] AU/ml vs. 147.4 [IQR, 27.5−3352.5] AU/ml, respectively; P = 0.0005). (c) Kidney transplant recipients being treated with steroids had lower median antibody titers compared with those who did not receive steroids (17.9 [IQR, 6.8−378.9] AU/ml vs. 74.8 [IQR, 7.2−2417.9] AU/ml; P = 0.002). (d) Kidney transplant recipients being treated with calcineurin inhibitors (CNIs) had lower median antibody titers compared with those who did not receive CNIs (18.1 [IQR, 6.8−330] AU/ml for patients under tacrolimus and 76.6 [IQR, 10.1−2392.2] AU/ml for patients under cyclosporine vs. 220 [IQR, 6.8−4269] AU/ml for patients who did not receive CNIs). (e) Kidney transplant recipients being treated with tacrolimus + antimetabolites (MMF/MPA) had lower median antibody titers compared with those did not (9.2 [IQR, 6.8−110.2] AU/ml vs. 90.9 [IQR, 7.7−1976] AU/ml, respectively; P < 0.0001). (f) Kidney transplant recipients being treated with tacrolimus + antimetabolites (MMF/MPA) + steroids had lower median antibody titers compared with those who did not (6.8 [IQR, 6.8−57.4] AU/ml vs. 79.4 [IQR, 6.9−1393.5] AU/ml, respectively; P < 0.0001). In summary, the immunization rate among KTRs who received 2 doses of the mRNA-1273 SARS-CoV-2 vaccine can be as low as 48%. The issue of a third vaccine dose in nonresponsive KTRs is an intriguing one that could be usefully explored in further research.
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