Immunogenicity of a Three-Dose Primary Series of mRNA COVID-19 Vaccines in Patients With Lymphoid Malignancies.

Background: Patients with lymphoid malignancies are at risk for poor coronavirus disease 2019 (COVID-19)-related outcomes and have reduced vaccine-induced immune responses. Currently, a 3-dose primary regimen of mRNA vaccines is recommended in the United States for immunocompromised hosts.
Methods: A prospective cohort study of healthy adults (n = 27) and patients with lymphoid malignancies (n = 94) was conducted, with longitudinal follow-up through completion of a 2- or 3-dose primary mRNA COVID vaccine series, respectively. Humoral responses were assessed in all participants, and cellular immunity was assessed in a subset of participants.
Results: The rate of seroconversion (68.1% vs 100%) and the magnitude of peak anti-S immunoglobulin G (IgG) titer (median anti-S IgG = 32.4, IQR = 0.48-75.0 vs median anti-S IgG = 72.6, IQR 51.1-100.1; P = .0202) were both significantly lower in patients with lymphoid malignancies compared to the healthy cohort. However, peak titers of patients with lymphoid malignancies who responded to vaccination were similar to healthy cohort titers (median anti-S IgG = 64.3; IQR, 23.7-161.5; P = .7424). The third dose seroconverted 7 of 41 (17.1%) patients who were seronegative after the first 2 doses. Although most patients with lymphoid malignancies produced vaccine-induced T-cell responses in the subset studied, B-cell frequencies were low with minimal memory cell formation. Conclusions: A 3-dose primary mRNA series enhanced anti-S IgG responses to titers equivalent to healthy adults in patients with lymphoid malignancies who were seropositive after the first 2 doses and seroconverted 17.1% who were seronegative after the first 2 doses. T-cell responses were present, raising the possibility that the vaccines may confer some cell-based protection even if not measurable by anti-S IgG.

Although two nanoparticle-encapsulated mRNA severe acute respiratory syndrome cornavirus 2 (SARS-CoV-2) vaccines—mRNA-1273 (Moderna, Inc.) and BNT162b2 (Pfizer BioNTech, Inc.)—have demonstrated high efficacy and safety for the general population [1, 2], the humoral and cellular kinetics in patients with lymphoid malignancies have not been well described after a primary series (three doses). We have previously described the humoral response after two doses in patients with lymphoid malignancies [3], which is consistent with additional studies of decreased immunogenicity in these patients [4, 5]. Underlying type of lymphoid malignancy and type and timing of therapy also impact SARS-CoV-2 antibody responses in these patients [6]. In particular, patients with lymphoid malignancies who have received specific therapies—such as anti-CD20 agents, Bruton tyrosine kinase (BTK) inhibitors, CD19-directed chimeric antigen receptor therapy (CAR-T), or stem cell transplantation—appear to have impaired humoral responses [7-9], although they may have some degree of cellular immunity [10, 11]. The degree of protection based on cellular immunity alone is not well described. Based on the existing data of poor immunogenicity in immunocompromised hosts with a two-dose mRNA series, the US Food and Drug Administration (FDA) amended the Emergency Use Authorization (EUA) to recommend a three-dose mRNA vaccine series (mRNA-1273 or BNT162b2) for immunocompromised hosts in August 2021 [12], which is now considered a primary series for this population. Few studies have evaluated the immunogenicity effects of a third dose for patients with hematological malignancies [13, 14], although data from a prospective registry (The Leukemia & Lymphoma Society National Registry, ClinicalTrials.gov Identifier NCT04794387) demonstrate that a third dose may produce a humoral response in a proportion of patients who had a suboptimal response to the first two doses [6].

There is an urgent need to better understand vaccine-induced immunogenicity in the context of heterogeneous host characteristics to improve protection for these patients who are at higher risk for poor outcomes from coronavirus disease 2019 (COVID-19). SARS-CoV-2 monoclonal antibody infusions have been a temporary solution for prevention, although this is a limited resource with short-lived efficacy due to immune escape mechanisms [15]. With limited tools in our current arsenal to protect immunocompromised patients against SARS-CoV-2, additional boosters have been approved [16], although these recommendations are based on imperfect data on a diverse range of immunocompromised hosts (eg, solid organ transplant recipients), which may not reflect the same immunodeficient characteristics as those with lymphoid malignancies. In addition, patients with lymphoid malignancies, and especially those receiving B cell-depleting therapies, often experience prolonged courses of SARS-CoV-2 infection that may play a key role in the generation of variant strains [17-19]. Thus, to generate optimal prevention strategies, the humoral and cellular aspects of immunity in this population and the nuanced effects of host characteristics and anticancer treatments must be better elucidated. In this study, we describe the SARS-CoV-2-specific immune humoral and cellular responses in a cohort of patients with lymphoid malignancies who received a primary series of three doses of mRNA COVID-19 vaccines. In the absence of a known correlate of protection, we compared these responses to the immunogenicity of a primary series (two doses of mRNA vaccines) in a cohort of healthy adults to further characterize the immune response.

METHODS

Study Population and Specimen Collection

A prospective cohort study was conducted at Brigham and Women’s Hospital (BWH) and Dana-Farber Cancer Institute (DFCI) from December 10, 2020 to February 15, 2022 with approval by the BWH and DFCI Institutional Review Board. All participants provided written informed consent, with eligibility and additional details in the Supplementary Materials. Participants were excluded at the time of enrollment if they had a prior history of COVID-19 or had received SARS-CoV-2 monoclonal antibodies. For the lymphoid malignancy cohort 1, patients were enrolled before first dose, with blood drawn at Day 0 (prevaccination), Day 21–28 (at the time of the second dose), Day 56, Day 112, and Day 196 as well as pre-third dose (up to 7 days before the third dose), 21–28 days after the third dose, and up to 3 months after the third dose. To increase the sample size, a separate cohort of patients (lymphoid malignancy cohort 2) were enrolled after the third vaccine dose was approved for immunocompromised individuals. In alignment with vaccination campaigns that were launched after the third dose approval, blood was collected at clinical satellite sites on the day of the third dose, 21–28 days after the third dose, and up to 3 months after the third dose. For the healthy cohort, blood was drawn at Day 0 (prevaccination), Day 21–28 (at the time of the second dose), Day 56, Day 112, and Day 196.

Serologic Assays: Simoa and Roche Elecsys Anti-Sars-CoV-2 S

The multiplexed, single-molecule array (Simoa) assay, quantitative detection of immunoglobulin G (IgG) antibodies against the Spike (S) protein and nucleocapsid (N) proteins were assessed for lymphoid malignancy cohort 1, with methods described previously [3, 20, 21]. The Simoa assay has a positivity threshold of 1.07 and 5.2 normalized average enzymes per bead (AEB) for anti-S IgG and anti-N IgG, respectively. The Roche Elecsys Anti-SARS-CoV-2 S assay, an electrochemiluminescence immunoassay, was used to analyze serum samples on the cobas c602 immunochemistry module in the lymphoid malignancy cohort 2 to assess total anti-S IgG [22]. The positive threshold is a cutoff index of ≥0.8 U/mL with an upper limit of 2500 U/mL. The samples from the healthy cohort were evaluated using both the Simoa and Roche assays. In this study, a “responder” was defined by any positive anti-S titer during the study period, according to the cutoff values for the given assay.

Cellular Immunity: Activation Induced Marker Assay

The activation induced marker (AIM) assay was adapted from protocols previously described [23, 24]. Flow cytometry was used to phenotype B and T cells after stimulation in the AIM assay. Fluorescent intensities were acquired using a LSRFortessa flow cytometer (Becton Dickinson) and data were analyzed using FlowJo software version 10. Additional details are in the Supplementary Materials.

Statistical Analyses

Median (interquartile range [IQR]) and Mann-Whitney U test were used to compare continuous variables. Count (percentage) and Fisher’s exact test were used to compare categorical variables. Correlation between months from CD20 therapy and anti-S IgG titer was evaluated using linear regression. Two-sided P values less than 0.05 were considered statistically significant. All analyses were conducted in R version 4.1.2 (https://www.R-project.org/).

RESULTS

Demographics and Disease Characteristics

Overall, 27 healthy participants and 103 patients with lymphoid malignancy were enrolled. Eight patients with lymphoid malignancy were excluded from the analysis due to receipt of non-mRNA COVID-19 vaccines during the study period, and 1 patient was excluded because he/she elected to terminate the study early. Therefore, a total of 94 participants were included in the analysis, with 41 participants in lymphoid malignancy cohort 1 and 53 participants in lymphoid malignancy cohort 2.

In the healthy cohort, 15 (56.0%) patients were female, and the median age 24.3 (IQR, 22.8–28.7), with 11 (40.7%) receiving 2 BNT162b2 (30 mcg) doses and 16 (59.3%) receiving 2 mRNA-1273 (100 mcg) doses. Only 1 participant in the healthy cohort had COVID-19 infection during the study period, with both a reported history and a positive anti-N IgG titer.

In the lymphoid malignancy combined cohort (n = 94), 49 (52.1%) were female, and the median age 65.5 was years (IQR, 57.5–72.8), with 56 (59.6) receiving 3 BNT162b2 (30 mcg) doses, 26 (27.7%) receiving 3 mRNA-1273 (100 mcg) doses, 2 (2.1%) receiving 2 BNT162b2 doses and 1 mRNA-1273 dose, and 7 (7.4%) receiving 2 mRNA-1273 doses and 1 BNT162b2 dose (Table 1). Three patients did not receive a third dose of mRNA vaccine due to clinician discretion, and 6 patients were not able to return to clinic for a post third dose blood draw. Most patients had an underlying diagnosis of chronic lymphocytic leukemia (CLL) (59, 62.8%), with 9 other lymphoma types represented (Table 1). The treatment status, defined as treatment naive, history of prior treatment (before the first vaccine dose), or active treatment (received treatment at any time after the first vaccine dose) was split among participants, 22 (23.4%), 27 (28.7%), 45 (47.9%), respectively, with specific treatments further characterized in Table 1.

Table 1.

Demographics and Disease and Treatment Characteristics

Characteristics	Healthy Cohort (n = 27)	Lymphoid Malignancy Cohort 1 (n = 41)	Lymphoid Malignancy Cohort 2 (n = 53)	Combined Lymphoid Malignancy (n = 94)
Female sex, n (%)	15 (56)	23 (52.3)	26 (49.1)	49 (52.1)
Age at vaccine dose 1, median (IQR)	24.3 (22.8–28.7)	68.4 (60.3–73.1)	63.0 (56.8–70.6)	65.5 (57.5–72.8)
Vaccine type[a] (first/second/third dose) n (%)
Pfizer/Pfizer/Pfizer	n/a	22 (53.7)	34 (64.2)	56 (59.6)
Moderna/Moderna/Moderna	n/a	11 (26.8)	15 (28.3)	26 (27.7)
Pfizer/Pfizer/Moderna	n/a	2 (4.9)	0 (0)	2 (2.1)
Moderna/Moderna/Pfizer	n/a	3 (7.3)	4 (7.5)	7 (7.4)
Pfizer/Pfizer	11 (40.7)	2 (4.9)	n/a	2 (2.1)
Moderna/Moderna	16 (59.3)	1 (2.4)	n/a	1 (1.1)
Median time between doses, days (IQR)
Between 1st and 2nd doses	28 (21–28)	21 (21–27)	22 (21–28)	21 (21–28)
Between 2nd and 3rd doses	n/a	168 (146–195)	167 (152–185)	168 (149–186)
History of COVID-19 infection during study period (reported or positive anti-N), n (%)	1 (3.7)	5 (12.2)	6 (11.3)	10 (10.6)
Median time (days) from third dose to postthird dose titer, (IQR)	n/a	45 (25.0–132.5)	27 (23–29)	28 (24–35)
Disease, n (%)
CLL	n/a	23 (56.1)	36 (64.3)	59 (62.8)
DLBCL	n/a	2 (4.9)	3 (5.7)	5 (5.3)
MCL	n/a	5 (11.6)	2 (3.8)	7 (7.4)
FL	n/a	3 (7.3)	4 (7.5)	7 (7.4)
MZL	n/a	2 (4.7)	2 (3.8)	4 (4.3)
HL	n/a	4 (9.3)	1 (1.9)	5 (5.3)
Angioimmunoblastic T-cell lymphoma	n/a	1 (2.4)	0	1 (1.1)
CNS Lymphoma	n/a	1 (2.4)	0	1 (1.1)
PLL	n/a	0	1 (1.9)	1 (1.1)
T-LGL	n/a	0	1 (1.9)	1 (1.1)
Treatment Status, n (%)
Treatment naive	n/a	9 (21.9)	13 (23.2)	22 (23.4)
Prior treatment	n/a	12 (29.3)	15 (26.8)	27 (28.7)
Active treatment	n/a	20 (48.8)	25 (44.6)	45 (47.9)
Treatment Groups, n (%)
Observation	n/a	9 (21.9)	13 (24.5)	22 (23.4)
BTKI[b]	n/a	10 (24.3)	10 (18.9)	20 (21.3)
Venetoclax monotherapy	n/a	5 (12.2)	3 (5.7)	8 (8.5)
CD20 Antibody therapy[c]	n/a	24 (58.5)	29 (54.7)	53 (56.4)
CD20 Ab within 12 months of 1st dose, n (%)	n/a	11/24 (45.8)	7/29 (24.1)	18/53 (34.0)
CD20 Ab beyond 12 months of 1st dose, n (%)	n/a	13/24 (54.2)	22/29 (75.9)	35/53 (66.0)
CD20 monotherapy	n/a	7 (17.1)	8 (15.1)	15 (16.0)
CD20 + BTKI	n/a	6 (14.6)	4 (7.5)	10 (10.6)
CD20 + venetoclax	n/a	5 (12.2)	5 (9.4)	10 (10.6)
CD20 + chemotherapy	n/a	1 (2.4)	11 (20.8)	12 (12.8)
CD20 + autologous stem cell transplant	n/a	2 (4.9)	0	2 (2.1)
CD20 + CAR-T cell therapy	n/a	3 (7.3)	1 (1.9)	4 (4.3)
Chemotherapy	n/a	2 (4.9)	3 (5.7)	5 (5.3)
Chemotherapy + autologous stem cell transplant	n/a	1 (2.4)	0	1 (1.1)
Autologous stem cell transplant	n/a	3 (7.3)	0	3 (3.2)
CAR-T cell therapy	n/a	3 (7.3)	1 (1.9)	4 (4.3)
Median number of prior lines of therapy (IQR)	n/a	2 (1–3)	1 (1–1)	1 (1–3)
IVIG during study period, n (%)	n/a	2 (4.8)	6 (10.7)	8 (8.5)
Median baseline IgG, mg/dL (IQR)	n/a	633 (483–937)	885 (708–969)	646 (489–938)

Abbreviations: Ab, antibody; BTKI, Bruton tyrosine kinase inhibitors; CAR-T, chimeric antigen receptor therapy; CLL, chronic lymphocytic leukemia; CNS, central nervous system; COVID-19, coronavirus disease 2019; DLBCL, diffuse large B-cell lymphoma; FL, follicular lymphoma; HL, Hodgkin’s lymphoma; IgG, immunoglobulin G; IQR, interquartile range; IVIG, intravenous immunoglobulin; MCL, mantle cell lymphoma; MZL, marginal zone lymphoma; n/a, not applicable; PLL, prolymphocytic leukemia; T-LGL, T-cell large granular lymphocytic leukemia;

100 mcg per dose for the Moderna vaccine and 30 mcg per dose for the Pfizer vaccine.

Bruton tyrosine kinase inhibitors: ibrutinib, acalabrutinib, Zanabrutinib, pirtobrutinib (LOXO-305).

CD20 antibody therapy includes the following: rituximab, Obinutuzumab. CD20 antibodies could be used as monotherapy or in combination with chemotherapy or targeted therapy.

Severe Acute Respiratory Syndrome Coronavirus 2 Infection During the Study Period

Eleven participants in the lymphoma cohorts and one participant in the healthy cohort developed COVID-19 infection during the study period, as determined by reported history, positive SARS-CoV-2 polymerase chain reaction in the electronic medical record, or positive anti-N IgG titer (Supplementary Table 1). Seven of the eleven lymphoma patients had a positive anti-S response to vaccination before infection, one seroconverted after infection, and two participants had no anti-S response before or after infection. One participant had no earlier titers (in the lymphoid group 2 cohort), and thus it is unknown whether post third dose titers were positive from infection or vaccination or both. The participant in the healthy cohort developed COVID-19 seven months after completing the two-dose vaccine series.

Seroconversion After Vaccination

All participants in the healthy cohort (27 of 27) had a positive response after the first mRNA COVID vaccine dose, which was maintained for the 6-month follow-up period, with modest antibody waning over time that was still maintained well above the positivity threshold (Figure 1). In contrast, there was a combined 68.1% seropositivity for patients with lymphoid malignancies (Supplementary Table 2, with breakdown of seropositivity by patient characteristics) after a three-dose series. In the lymphoid malignancy cohort 1, 14 of 41 (34.1%) had a positive anti-S titer after the first dose, 22 of 41 (53.7%) were positive after the second dose, and 22 of 32 (68.8%) were positive after the third dose. Patients did not necessarily maintain a positive response over time, with evidence of seroreversion. Only two participants who were seronegative after the first two doses had seroconversion after the third dose, with low titers (median anti-IgG = 6.55 nAEB; IQR, 3.82–9.28). Of the 22 of 53 participants in lymphoid malignancy cohort 2 who were seronegative before receipt of the third dose, only five seroconverted after receiving a third dose, with an overall low median titer of 123.5 U/mL (IQR, 100.9–357.7).

Figure 1.

Anti-S IgG titers from the time of first vaccine dose (day 0) to 6 months after series completion (through day 205) in healthy participants (n = 27). The dotted line at 1.07 represents the positivity threshold for the Simoa assay.

Anti-S Immunoglobulin G Responses After First and Second Doses

There was greater variability in the lymphoid malignancy cohort 1 after the first and second doses compared to the healthy controls (Figure 2). At 21–28 days post first dose, the median anti-S IgG titer was 25.5 (IQR, 14.4–38.1) compared to 0.1 (IQR, 0.1–1.6) in the healthy cohort and the lymphoid malignancy cohort 1, respectively (P < .001), with significantly lower titers at days 49–56 (post second dose) and days 168–250 as well (Table 2). Even among the responders (n = 28) with lymphoid malignancies (Figure 2), the magnitude of response was significantly lower at 21–28 days (median anti-S IgG = 0.8; IQR, 0.1–8.5), 49–56 days (post second dose; median anti-S IgG = 27.2; IQR, 9.4–49.5), and 168–250 days (anti-S IgG = 2.4; IQR, 0.6–11.7) compared to the healthy cohort (median anti-S IgG = 25.5 and IQR = 14.4–38.1, median anti-S IgG = 70.3 and IQR = 49.7–95.8, and median anti-S IgG = 17.1 and IQR = 10.4–25.0, respectively) (Table 2).

Figure 2.

Anti-S IgG titers from the time of first vaccine dose (day 0) to day 420 in all participants in the lymphoid malignancy cohort 1 (n = 41; A) and only the responders (n = 28) in lymphoid malignancy cohort 1 (B). Pink dots represent titers drawn from day 0 through post second dose titers; blue dots represent titers drawn after the third vaccine dose. The dotted line at 1.07 represents the positivity threshold for the Simoa assay.

Table 2.

Median Anti-S IgG Titers Over Time in Healthy Adults vs Lymphoid Malignancy Cohort 1

Simoa Assay (Normalized AEB)	Healthy Cohort (n = 27)	Lymphoid Malignancy Cohort 1 (n = 41)	Cohort 1: Responders Only (n = 28)	P Value (Healthy vs Cohort 1)	P Value (Healthy vs Responders Only)
21–28 days postfirst dose, median (IQR)	25.5 (14.4–38.1)	0.1 (0.1–1.6)	0.8 (0.1–8.5)	P < .001	P < .001
49–56 days postfirst dose, median (IQR)	70.3 (49.7–95.8)	15.3 (0.6–39.4)	27.2 (9.4–49.5)	P < .001	P < .001
168–250 days postfirst dose, median (IQR)	17.1 (10.4–25.0)	0.6 (0.6–5.6)	2.4 (0.6–11.7)	P < .001	P < .001
Postseries completion[a], median (IQR)	72.6 (51.1–100.1)	32.4 (0.48–75.0)	64.3 (23.7–161.5)	P = .0202	P = .7424

Abbreviations: AEB, average enzymes per bead; IgG, immunoglobulin G; IQR, interquartile range.

Postseries completion titers were taken ∼1–2 months after the 2-dose series (healthy cohort) or 3-dose primary series (lymphoid malignancy cohort).

Anti-S Immunoglobulin G Responses After a Third Dose

After the third dose (median 45 days; IQR, 25–132.5), the median anti-S IgG for the entire lymphoid malignancy cohort 1 (median anti-S IgG = 32.4; IQR, 0.48–75.0) and the responders (median anti-S IgG = 64.3; IQR, 23.7 –161.5) was compared to the healthy cohort 28 days after a 2-dose series completion (median anti-S IgG = 72.6; IQR, 51.1–100.1) (Table 2). The median titer was significantly lower in lymphoid malignancy cohort 1 (P = .0202) but not significantly different for the responders (P = .7424), indicating that the responders were able to achieve similar titer levels to the healthy cohort after the third dose.

In the lymphoid malignancy cohort 2, anti-S total IgG titers after the third dose were collected clinically using the Roche assay. The median time from the anti-S IgG titer from the third dose was 27 days (IQR, 23–29), with a median anti-S IgG titer of 670 U/mL (IQR, 0–2500) for all patients and 2500 U/mL (IQR, 592–2500) for the responders. In comparison, the median anti-S IgG titer in the healthy cohort was 2500 U/mL (IQR, 1933.5–2500) at 28 days after a 2-dose series completion, which is significantly higher compared to the entire cohort 2 (P = .0032) but not significantly different compared to the responders only (P = .4574) (Supplementary Table 3), similar to the results described for cohort 1.

Responders by Treatment in the Lymphoid Malignancy Cohorts

Patients who were treatment naive had a higher rate of response (95.5%) compared to those who had received prior treatment (70.4%) or were actively receiving therapies (53.3%) during the study period. Within the treatment groups, participants who received prior or active venetoclax monotherapy, CAR-T therapy, CD20 antibody monotherapy, or combination of venetoclax and CD20 therapy had the lowest rates of response (50.0%, 50.0%, 40.0%, and 30.0%, respectively). There was a positive although nonsignificant correlation between months from CD20 therapy and anti-S IgG titer (r2 = 0.1035, P = .125) (Supplementary Figure 1), in which the highest anti-S IgG titer was selected for each participant who had received any CD20 therapy in the past, with a stronger linear correlation observed in participants who had received CD20 monotherapy only (r2 = 0.58, P = .0454) (Supplementary Figure 1).

B- and T-Cell Immunophenotyping Results

A subset of the overall lymphoid malignancy cohort (Supplementary Table 4) opted to have additional blood drawn for cellular analyses (n = 17) up to the third dose. Quantification of circulating S protein-specific B cells by flow cytometry confirmed that vaccine-induced B cells could be observed in some of the participants after the first and second immunizations (Figure 3). Phenotypic analysis of these B cells shows that the absence in increased B-cell frequency coincides with an impairment in class-switch recombination and memory formation, as indicated by the absence of vaccine-specific IgD-CD27+ B cells (Supplementary Figure 2). In contrast to the frequency of vaccine-induced B cells, an appreciable increase in vaccine-induced CD4+ and, in particular, CD8+ T cells was observed after the first and second immunization (Figure 3 and ). Phenotypic analysis reveals that vaccine-specific T cells were of antigen-experienced phenotype (CD62L-negative) and capable of producing interleukin (IL)-2 and interferon (IFN)-γ after stimulation with antigenic peptides (Supplementary Figure 2 and ). In the cellular subset, 9 of 17 (52.9%) had a positive anti-S IgG response (Supplementary Table 4). It is interesting to note that among the eight participants in the cellular subset who had no anti-S IgG response, seven had vaccine-induced CD4+ and CD8+ responses and produced IL-2 and IFN-γ after stimulation with antigenic peptides. Both B- and T-cell frequencies waned over time.

Figure 3.

The percentage frequency of Spike-specific B cells (A), CD4+ cells (B), and CD8+ cells (C) are shown. A subset of participants from both lymphoid malignancy cohort 1 and 2 (n = 17) had cellular responses assessed at baseline (the time of dose 1; Visit 1), 21–28 days later (the time of dose 2; Visit 2), 49–56 days later (1 month after dose 2; Visit 3), and 5–6 months later (the time of dose 3; Visit 4). Prepandemic samples were run as controls and shown on the left.

DISCUSSION

In this study, we describe the kinetics of anti-S IgG response through a three-dose primary mRNA series in patients with lymphoid malignancies and found a decreased median humoral response compared to a two-dose primary mRNA series in healthy individuals, with only 68.1% patients with lymphoid malignancy seroconverting at any point during the study period. Although others have also described decreased seroconversion in patients with lymphoid malignancies after SARS-CoV-2 vaccination [14], our study is unique in evaluating the humoral responses longitudinally through a third dose and comparing to a healthy cohort, as well as in evaluating cellular responses over time in a highly characterized cohort.

Seroconversion rates alone do not fully capture the quantity and quality of the humoral response nor timing of seroconversion, all important aspects of vaccine immunogenicity. In our study, only a small number of patients with lymphoid malignancy who did not respond to the first two doses seroconverted after a third dose. Although this may still support the use of a third dose to increase the number of responders, those who seroconverted after the third dose had low titers, which may not confer strong protection. Furthermore, a positive antibody response at one point in time does not predict a sustained response in this population, as seen for the participants in our study who had waning antibody over time. Possible explanations may include lack of memory B-cell formation, rapid waning of antibody, and/or specific immunosuppressive therapies given after the vaccine dose.

However, among participants in the lymphoid malignancy cohort who seroconverted after the first 2 doses, 3 doses were needed to achieve similar titer levels to those in the healthy cohort post series, supporting the use of a third dose for this subset of patients. Although correlates of protection for SARS-CoV-2 vaccines have not yet been clearly defined [25], the comparison of titer levels to the healthy controls offers more insight to the degree of protection (rather than seroconversion alone) based on available evidence from phase 3 trials [26].

With respect to cellular immunity, some participants demonstrated an increased frequency of S-positive B cells after vaccination although generally low, which is not unexpected given B cell-directed therapies. However, most demonstrated increased frequencies of vaccine-induced CD4+ and CD8+ cells, consistent with other studies of immunocompromised hosts [13, 27]. We found that among participants in the cellular subset who had no humoral response, most were able to produce vaccine-induced CD4+ and CD8+ responses. Thus, patients with lymphoid malignancy receiving mRNA vaccines may have partial protection due to cellular immunity, even in the absence of a humoral response. However, the durability of this response could be short lived, with decreasing frequencies in the periphery observed for both B- and T-cells at 5 to 6 months post second doses of vaccine. Alternatively, the decrease in peripheral frequency could be the result of homing to tissue or lymph node, thus potentially improving durability, if T-cells have a high CCR7 expression [28, 29]. Further studies should evaluate whether additional vaccine doses can bolster cellular immunity or induce a more durable T-cell response and determine how cellular immunity correlates with clinical efficacy against severe COVID-19.

Limitations of this study include the relatively small sample size, precluding assessment of potential differences in humoral or cellular responses based on age, vaccine type, disease characteristics, or treatments. However, we were able to demonstrate important trends by disease type and treatments, which should be further explored in larger studies. Although we used two different assays to measure anti-S IgG response, we have previously demonstrated high concordance between the Simoa and Roche assays [9]. Future studies should address the clinical efficacy and the role of both humoral (including neutralization) and cellular immunity in conferring protection against COVID-19 in patients with lymphoid malignancies. Due to the timing of our study, third doses for immunocompromised hosts were not available until approximately six months after the first two mRNA vaccine doses were administered. Thus, in our cohort, the median time between the second and third dose was 168 days (IQR, 146–195). The Centers for Disease Control and Prevention now recommends that immunocompromised hosts may receive the third dose of the primary series as early as one month after the second dose [30]. Our study does not assess how the timing of the third dose may affect antibody response, nor how additional boosters (fourth or fifth doses) may affect immunity; these variables will be important to assess for future studies.

CONCLUSIONS

In summary, although a primary series of three doses of mRNA vaccines is currently recommended in the United States for immunocompromised hosts, our study demonstrates that the third dose only bolsters humoral responses in those who could produce an endogenous response to one or two doses, with a similar magnitude of titer compared to healthy individuals after a primary series. However, as has been described in solid organ transplant recipients [31], a third dose did not induce substantial seroconversion among those who were seronegative after the first 2 doses, nor did it dependably convert those who had seroreverted. In addition, T-cell immunity was induced, even in those without a humoral response. Thus, measuring antibody responses alone may not be a full measure of SARS-CoV-2 protection.

Given the increasing appreciation of the variation in immunity between individuals, we are entering an era of precision vaccinology [32]. In this context, future vaccination recommendations must consider specific host characteristics of patients with lymphoid malignancies, avoiding a classification of this subpopulation under a generic umbrella of “immunocompromised hosts.” Precision immunization strategies to protect this vulnerable population according to disease, prior anticancer therapeutics, and other host characteristics are urgently needed to provide improved protection and reduce prolonged SARS-CoV-2 shedding, thereby providing broader public health benefits by curbing the pandemic and potentially reducing generation of variant strains.

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