key: cord-0703310-n5ku1txk
authors: Haarhaus, Mathias; Duhanes, Monica; Leševic, Nataša; Matei, Bogdan; Ramsauer, Bernd; Da Silva Rodrigues, Rui; Su, Jun; Haase, Michael; Santos‐ Araújo, Carla; Macario, Fernando
title: Improved immunologic response to COVID‐19 vaccine with prolonged dosing interval in haemodialysis patients
date: 2022-03-07
journal: Scand J Immunol
DOI: 10.1111/sji.13152
sha: 2f997941c2f32afb24c454df6f1ff33ed63110c2
doc_id: 703310
cord_uid: n5ku1txk

Vaccination against 2019 coronavirus disease (COVID‐19) can reduce disease incidence and severity. Dialysis patients demonstrate a delayed immunologic response to vaccines. We determined factors affecting the immunologic response to COVID‐19 vaccines in haemodialysis patients. All patients within a Swedish haemodialysis network, vaccinated with two doses of COVID‐19 vaccine 2‐8 weeks before inclusion, were eligible for this cross‐sectional study. Severe adult respiratory syndrome coronavirus 2 (SARS‐CoV‐2) spike protein antibody levels were determined by EliA SARS‐CoV‐2‐Sp1 IgG test (Thermo Fisher Scientific, Phadia AB) and related to clinical and demographic parameters. Eighty‐nine patients were included. Patients were vaccinated with two doses of Comirnaty (BNT162b2, 73%) or Spikevax (mRNA‐1273, 23,6%). Three patients received combinations of different vaccines. Response rate (antibody titres >7 U/mL) was 89.9%, while 39.3% developed high antibody titres (>204 U/mL), 47 (43‐50) days after the second dose. A previous COVID‐19 infection associated with higher antibody titres (median (25th‐75th percentile) 1558.5 (814.5‐3,763.8) U/mL vs 87 (26‐268) U/mL, P = .002), while time between vaccine doses did not differ between groups (P = .7). Increasing SARS‐CoV‐2 antibody titres were independently associated with increasing time between vaccine doses (B 0.241, P = .02), decreasing serum calcium levels (B −0.233, P = .007) and previous COVID‐19 (B 1.078, P < .001). In conclusion, a longer interval between COVID‐19 mRNA vaccine doses, lower calcium and a previous COVID‐19 infection were independently associated with a stronger immunologic vaccination response in haemodialysis patients. While the response rate was good, only a minority developed high antibody titres, 47 (43‐50) days after the second vaccine dose.

39.3% developed high antibody titres (>204 U/mL), 47 (43-50) days after the second dose. A previous COVID-19 infection associated with higher antibody titres (median (25th-75th percentile) 1558.5 (814.5-3,763.8) U/mL vs 87 (26-268) U/ mL, P = .002), while time between vaccine doses did not differ between groups (P = .7). Increasing SARS-CoV-2 antibody titres were independently associated with increasing time between vaccine doses (B 0.241, P = .02), decreasing serum calcium levels (B −0.233, P = .007) and previous COVID-19 (B 1.078, P < .001).

In conclusion, a longer interval between COVID-19 mRNA vaccine doses, lower calcium and a previous COVID-19 infection were independently associated with a stronger immunologic vaccination response in haemodialysis patients. While the response rate was good, only a minority developed high antibody titres, 47 (43-50) days after the second vaccine dose.

Patients with chronic kidney disease (CKD) are especially vulnerable to infection with 2019 coronavirus disease (COVID-19) and develop more often serious complications than other populations. 1 Dialysis patients have therefore been granted high priority in the roll-out of COVID-19 vaccination campaigns in many countries. Several studies have reported an impaired humoral immunologic response to COVID-19 vaccines 2,3 and a prolonged time to peak levels of severe adult respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein IgG antibodies in dialysis patients after COVID-19 vaccination. 2, 4 Optimal timing of vaccine doses has become an important topic of discussion. An improved immunologic response with prolongation of the time interval between dose one and dose two of Vaxzevria and Comirnaty has been described in non-CKD populations. 5, 6 An effect of variable time intervals between the first and second vaccine dose on the immunologic response has not yet been described in dialysis patients. We studied the effect of a prolongation of the interval between the first and second dose of COVID-19 vaccines on the humoral immunologic response in haemodialysis patients. Most patients in the current study received two doses of mRNA vaccine (Comirnaty, BNT162b2, Pfizer/BioNTech or Spikevax, mRNA-1273, and Moderna), but one patient received a combination of mRNA and a vectorbased vaccine (Comirnaty and Vaxzevria, ChAdOx-1 and AstraZeneca). Manufacturers' recommendations for the time between doses are 3 weeks for Comirnaty and 4 weeks for Spikevax. However, Swedish health authorities recommend dose intervals of 3-7 weeks for the Comirnaty vaccine and 4-7 weeks for the Spikevax vaccine. Thus, the time gap between vaccine doses varied for patients treated at the participating dialysis centres in the current study.

The current cross-sectional study was performed in five haemodialysis outpatient clinics in Central Sweden. All 198 maintenance haemodialysis patients were screened for inclusion. Patients who had received vaccination with two doses of COVID-19 vaccine and timing of the second dose 2-8 weeks prior to study start were included in the study after written informed consent. Clinical and demographic data, including routine laboratory data within ±4 weeks from blood sampling, for anti-SARS-CoV-2 spike protein antibodies were retrieved from the Renal Information Management System (iRIMS), a quality registry, collecting dialysis-related data prospectively. The study was approved by the Swedish Ethical Review Authority (2021-01442).

Blood samples for anti-SARS-CoV-2 spike protein IgG antibodies were collected before a haemodialysis session. Titres of anti-SARS-CoV-2 IgG antibodies in serum were determined using the EliA SARS-CoV-2-Sp1 IgG test (Thermo Fisher Scientific, Phadia AB). The assay was performed according to the manufacturer's instructions. Results <7 U/mL were considered negative and antibody titres >204 U/mL were considered strongly positive according to manufacturer's definition.

Data are presented as median (25th-75th percentiles), frequencies or percentages, if not stated otherwise. A Pvalue below 0.05 was considered significant. Patients with a previous COVID-19 diagnosis were compared with COVID-19 naïve patients. Furthermore, we compared patients according to the type of vaccine they had received. We applied the independent-samples median test for paired comparisons and for multiple comparisons with the Bonferroni correction for post hoc analyses. For correlation and regression analyses, continuous variables were standardized with outliers replaced by three standard deviations. Univariate correlations were calculated using Spearman's Rho correlation coefficient, and multivariate analyses were performed using linear regression. Covariates for the determination of anti-SARS-CoV-2 spike protein antibody levels 2-8 weeks after the second vaccination were chosen, based on a P < .2 in univariate correlations and/or clinical relevance. Missing data were excluded pairwise or listwise. Sensitivity analyses were performed, including also patients with vaccination interval outside of the recommended range.

Of the 198 screened patients, 98 had received 2 vaccine doses, with the last dose 2-8 weeks before inclusion. Two patients refused consent. Of 96 patients with two doses of COVID-19 vaccine, who consented to participate in the current study, 4 patients were excluded due to unreliable anti-SARS-CoV-2 spike protein antibody results and 3 patients were excluded, since the interval between the first and second vaccine dose was outside of the range recommended by Swedish authorities. Demographic and clinical data of the remaining 89 patients are listed in Table 1 .

Patients were either vaccinated with two doses of Comirnaty (N = 65), two doses of Spikevax (N = 21) or combinations of different vaccines (N = 3). Median interval between vaccine dose 1 and dose 2 was 24 (minimum 21 -maximum 45) days, and median anti-SARS-CoV-2 spike protein antibody level was 114.0 (27.0-430.5) U/mL. While median time between the first and second doses Table 2 . Multivariate analysis of all patients revealed independent associations of an increasing time interval between the first and second vaccine doses, a history of COVID-19, and lower serum calcium levels with a stronger immunologic vaccine response (Table 3) . Sensitivity analyses, including also patients with vaccination intervals outside of the recommended range, revealed similar results (Tables S1 and Table S2 ).

The current study demonstrates for the first time an independent association of a longer interval between two COVID-19 vaccine doses with a stronger anti-SARS-CoV-2 spike protein IgG antibody response in haemodialysis patients. Our findings are in line with previous reports of an improved immunologic response to a delay of the second vaccine dose in non-CKD patients. 5 the improved immunologic response associated with a longer interval between the first and second vaccine doses in the current study may be due to a delayed immunologic response, possibly related to differences in the immune system of haemodialysis patients, that might affect the affinity maturation process and the magnitude of the antibody response.

Prolongations of vaccination intervals up to several months have been suggested by health administrations, not only to achieve an improved immunologic response, but also to meet vaccine shortages. However, recently, such long prolongations have been questioned, due to the risk of insufficient protection after a single vaccine dose, especially against rapidly spreading new variants. 8 Although antibodies are just one of several components implicated in protective immunity to SARS-CoV-2, increasing evidence shows that measured immunity correlates with clinical protection against symptomatic and asymptomatic SARS-CoV-2 infection. 9 It is thus reassuring that we saw an improved humoral immunologic response in the current study in spite of a short prolongation of the interval between vaccine dose 1 and dose 2, which was at maximum 45 days.

Seroconversion rate was 89.9% with no significant difference in antibody levels between Comirnaty, Spikevax or combinations of different vaccines. This finding is in line with previous reports. 2, 3 The fact, that a considerably lower proportion of patients achieved a strong antibody response in the current and in previous studies 2, 3 suggests, that dialysis patients may need a third booster dose, to achieve high antibody titres. Interestingly, a recent report from a French dialysis cohort demonstrated an impressive improvement of antibody titres one month after a third vaccine dose in haemodialysis patients with a sub-optimal immunologic response after 2 doses of the Comirnaty vaccine. 10 We found a strong association between a previous COVID-19 infection and a more robust immunologic response to COVID-19 vaccines, which confirms earlier reports. 7, 11 The most likely mechanism could be a rapid reactivation of the immunological memory to SARS-CoV-2 by COVID-19 vaccines. 7, 12 However, the accelerated decline in serum levels of anti-SARS-CoV-2 antibodies after a previous COVID-19 infection in dialysis patients 13 may indicate that a single vaccine dose for patients with a previous COVID-19 infection, as suggested for general populations by Mazzoni et al, 12 may not be sufficient in dialysis patients.

Experimental and clinical evidence for a modulation of vaccine responses by serum calcium in advanced CKD is few and divergent. A high-calcium diet has been shown to improve the immune response to tetanus vaccine in uremic rats. 14 On the contrary, treatment of dialysis patients with paricalcitol did not improve the response to a standard booster dose of hepatitis B vaccine, in spite of increasing serum calcium levels. 15 Thus, our finding of an association of lower serum calcium levels with a stronger immune response to COVID-19 vaccines is hypothesis generating, but needs to be confirmed by additional studies.

Limitations of the current study are the observational and cross-sectional character, which does not allow any causative deductions. Further limitations are the relatively small number of participants, the lack of clinical data on SARS-CoV-2 infections after vaccination and the lack of baseline samples for determination of anti-SARS-CoV-2 spike protein antibodies. The timing of the blood samples in the current study is somewhat later than the expected early peak of antibody levels after the second dose of COVID-19 vaccine in general populations. 16 However, it is in accordance with the peak AB responses in a previous kinetic study in haemodialysis patients 4 and a systematic review of antibody studies in haemodialysis patients. 2 In conclusion, we demonstrate an independent association of a longer time interval between the first and second dose of COVID-19 vaccines with a better immunologic response in maintenance haemodialysis patients. Our findings may aid in future development of vaccination strategies for dialysis patients in face of variable access to COVID-19 vaccines.

Risk prediction of COVID-19 incidence and mortality in a large multi-national hemodialysis cohort: implications for management of the pandemic in outpatient hemodialysis settings

Review of early immune response to SARS-CoV-2 vaccination among patients with CKD

Timedependent evolution of IgG antibody levels after first and second dose of mRNA-based SARS-CoV-2 vaccination in hemodialysis patients: a multicenter study

Antibody response to the BNT162b2 vaccine in maintenance hemodialysis patients

Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials

Immunogenicity of standard and extended dosing intervals of BNT162b2 mRNA vaccine

Immunogenicity of a first dose of mRNA-or vector-based SARS-CoV-2 vaccination in dialysis patients: a multicenter prospective observational pilot study

Effectiveness of Covid-19 Vaccines against the B.1.617.2 (Delta) Variant

Correlates of protection against symptomatic and asymptomatic SARS-CoV-2 infection

COVID-19 Vaccination in Haemodialysis Patients: Good things come in threes…

Immunogenicity of SARS-CoV-2 vaccine in dialysis

First-dose mRNA vaccination is sufficient to reactivate immunological memory to SARS-CoV-2 in subjects who have recovered from COVID-19

Antibody status, disease history, and incidence of SARS-CoV-2 infection among patients on chronic dialysis

Treatment of hyperphosphatemia, secondary hyperparathyroidism and hypocalcemia with calcium carbonate favorably modulates vaccination response in uremic rats

A placebo-controlled trial to evaluate immunomodulatory effects of paricalcitol

BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells in humans

The current study was supported by Diaverum Sweden AB. We thank the study participants and healthcare personnel at the participating centres for their excellent cooperation.

MaH, MD, NL, BM, BR, MiH, CS and FM are employees of Diaverum. MaH is clinical advisory board member of Resverlogix, unrelated to the submitted work. RDR and JS have nothing to declare.

Written informed consent was obtained from all subjects. The study protocol complied with the Declaration of Helsinki and its amendments. The study was approved by the Swedish Ethical Review Authority (2021-01442).

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Mathias Haarhaus https://orcid. org/0000-0001-8274-6356