SARS-CoV-2 Antibody Avidity Responses in COVID-19 Patients and Convalescent Plasma Donors.

BACKGROUND: Convalescent plasma therapy is a leading treatment for conferring temporary immunity to COVID-19-susceptible individuals or for use as post-exposure prophylaxis. However, not all recovered patients develop adequate antibody titers for donation and the relationship between avidity and neutralizing titers is currently not well understood.
METHODS: SARS-CoV-2 anti-spike and anti-nucleocapsid IgG titers and avidity were measured in a longitudinal cohort of COVID-19 hospitalized patients (n = 16 individuals) and a cross-sectional sample of convalescent plasma donors (n = 130). Epidemiologic correlates of avidity were examined in donors by linear regression. The association of avidity and a high neutralizing titer (NT) were also assessed in donors using modified Poisson regression.
RESULTS: Antibody avidity increased over duration of infection and remained elevated. In convalescent plasma donors, higher levels of anti-spike avidity were associated with older age, male sex, and hospitalization. Higher NTs had a stronger positive correlation with anti-spike IgG avidity (Spearman ρ = 0.386; P < .001) than with anti-nucleocapsid IgG avidity (Spearman ρ = 0.211; P = .026). Increasing levels of anti-spike IgG avidity were associated with high NT (≥160) (adjusted prevalence ratio = 1.58 [95% confidence interval = 1.19-2.12]), independent of age, sex, and hospitalization.
CONCLUSIONS: SARS-CoV-2 antibody avidity correlated with duration of infection and higher neutralizing titers, suggesting a potential alternative screening parameter for identifying optimal convalescent plasma donors.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the cause of coronavirus disease (COVID-19), was declared a pandemic in early 2020 by the World Health Organization [1, 2]. As of 1 September 2020, there have been over 25 million confirmed COVID-19 cases and over 840 000 deaths [2, 3]. Symptoms of COVID-19 include cough, fever, fatigue, muscle pain, and shortness of breath, with hospitalized patients at higher risk of death [2-4].

Currently, there remains no prophylactic vaccine for SARS-CoV-2 infection and pharmaceutical therapeutics are limited. Convalescent plasma therapy is presently the best option to confer temporary immediate passive immunity for infection prevention or early treatment of individuals [5]. Historically, passive immune therapy has been used as post-exposure prophylaxis or hospital treatment for a variety of viral infections [5-9]. Observational studies have evaluated the use of convalescent plasma to treat COVID-19, suggesting both safety and efficacy, as reflected by shortened duration of hospitalizations and lower mortality (ie, as compared to nontransfused controls) [6-11].

Neutralizing antibodies in convalescent individuals are of major interest as they bind to various viral epitopes, inhibiting infectivity by blocking attachment or entry into host cells [12]. While the US Food and Drug Administration (FDA) initially did not require neutralizing antibody titer testing for potential convalescent plasma donors at the beginning of the pandemic, they recommended a target titer of > 1:320 for ideal donors if testing was available; this target titer was subsequently lowered [5, 13]. Additionally, 30% of recovered patients have low titers of SARS-CoV-2–specific neutralizing antibodies and > 5% have undetectable levels [5, 14]. Determinants of SARS-CoV-2 neutralizing antibody responses are largely unknown.

Of the 4 main structural SARS-CoV-2 proteins, spike (S1 subunit and receptor binding domain) and nucleocapsid proteins are the most immunogenic [15, 16]. In recent studies, potent antiviral receptor binding domain specific antibodies were found in all COVID-19 convalescent plasma donors despite low titers of neutralizing antibodies [17]. While the overall antibody titer is most likely an important factor in determining the viral neutralization potential of a given convalescent plasma donor, multiple other factors likely play a role. These include antibody binding avidity, diversity of response, and amounts of differing antibody classes. While antibody avidity, combined strength of the antibody-antigen complex, can have substantial impact on the humoral immune response, there are limited data on temporal dynamics and correlates of SARS-CoV-2 antibody avidity responses, and whether a stronger avidity response is associated with higher neutralizing titers. An association between antibody avidity and neutralizing antibody titer may also help to identify optimal convalescent plasma donors.

The aim of this study was to characterize SARS-CoV-2 immunoglobulin G (IgG) antibody titers and avidity responses in acute and convalescent patients, and compare their association with neutralizing antibody titers.

METHODS

Study Sample

Longitudinal COVID-19 Sample Patients

All patients had confirmed SARS-CoV-2 infection via a positive RNA nasopharyngeal swab and a known date of symptom onset. Discarded blood serum samples were collected from specimens sent for clinical testing of patients over the duration of their inpatient stay. Samples were selected from individuals with multiple time points available after observed seroconversion. In total 16 distinct hospitalized patients at the Johns Hopkins Hospital contributed 84 serum samples with a median of 5 samples per patient (range, 2–8; interquartile range [IQR], 4.5–6.0).

Convalescent Plasma Donors

Recovered COVID-19 patients were contacted by study personnel to determine interest in donating convalescent plasma. All subjects had confirmed infection of SARS-CoV-2 determined by a positive reverse transcription polymerase chain reaction (RT-PCR) of a nasopharyngeal swab. All potential donors had to be at least 18 years old and meet criteria for blood donation (ie, never been diagnosed with human immunodeficiency virus [HIV], not pregnant, etc.). Potential donors had 25 mL of whole blood collected. Blood was separated into plasma and peripheral blood mononuclear cells within 12 hours of collection, and plasma samples were aliquoted and stored at −80°C. All donors provided informed written consent.

Ethics Statement

Studies of both cohorts were approved by The Johns Hopkins University School of Medicine Institutional Review Board.

Laboratory Testing

Neutralizing Antibody Titers

Quantitation of neutralizing antibody titers against 100 fifty percent tissue culture infectious doses was performed using a microneutralization (NT) assay, as previously described [18, 19]. Endpoint NT titers were calculated as the highest serum dilution that eliminated cytopathic effect in 50% of the wells (ie, 3 of 6 replicate wells). NT area under the curve (AUC) values were estimated using the exact number of wells protected from infection at every plasma dilution; samples that had no NT activity were assigned a value of one-half of the lowest NT AUC. For analytic purposes in this study, NT AUC values ≥ 40 were considered to indicate moderate neutralization potency and NT AUC values ≥ 160 were considered to indicate high neutralization potency [13].

Enzyme-Linked Immunosorbent Assays

Euroimmun anti-SARS-CoV-2 IgG enzyme-linked immunosorbent assay (ELISA) for the S1 domain of spike protein and EDI Novel Coronavirus COVID-19 IgG ELISA (Epitope Diagnostics Inc.) for nucleocapsid protein were performed per the manufacturers’ protocols. For Euroimmun, optical density (OD) of the sample divided by calibrator provided arbitrary unit (AU) ratio for which ≥ 1.1 were considered positive and ≥ 0.8–1.1 were considered indeterminate. For EDI, normalized optical density (ODn) ≥ 0.22 were considered positive and ≥ 0.18 were considered indeterminate.

Avidity Enzyme-Linked Immunosorbent Assays

Avidity assays were performed for samples that had Euroimmun AU ratios ≥ 0.8 and EDI ODns ≥ 0.18 (ie, indeterminates and seropositive specimens). Euroimmun anti-SARS-CoV-2 ELISA IgG kits and EDI Novel Coronavirus COVID-19 IgG ELISA kits were used with modified protocols for avidity testing [19]. Each reaction utilized the following components: 100 µL of diluted plasma (1:101 dilution for Euroimmun or 1:100 dilution for EDI per manufacturers’ protocols), and 100 µL of undiluted positive, negative, or calibrator controls. Plates containing reaction components were incubated either for 1 hour at 37°C followed by 3 washes (Euroimmun) or 30 minutes at room temperature followed by 5 washes (EDI). Urea, 300 µL, diluted in the appropriate wash buffer at varying concentrations (0, 1, 2, 4, 6, and 8 M) were added to the plates and incubated at 37°C for 10 minutes [20]. Plates were washed 3 or 5 times followed by manufacturer’s protocol for addition of conjugate and substrate. Ratios of sample with urea concentration to sample without urea (either AU or ODn) were used to calculate dissociation constant (DC50). The DC50 was the concentration of urea where 50% of the signal was lost (Supplementary Figure 1). In samples where 50% of the signal was not lost by 8 M urea solution, samples DC50 were truncated at 8. DC50 calculations were performed using AAT Bioquest IC50 calculator using 4 parameter logistic regression model [21].

Statistical Analysis

Descriptive statistics were used to characterize both study populations: the longitudinal cohort of hospitalized COVID-19 patients and the cross-sectional sample of COVID-19 convalescent plasma donors. Percentages were calculated for categorical variables and continuous variables were described with medians and corresponding interquartile ranges (IQR). The primary study outcomes included anti-spike IgG avidity and anti-nucleocapsid IgG avidity as measured by the Euroimmun and EDI assays, respectively. Longitudinal trajectories in IgG titers and avidity outcomes were visualized by spaghetti plots and examined descriptively by time since symptom onset in the cohort of hospitalized COVID-19 patients. The remaining statistical analyses were conducted among the sample of convalescent plasma donors.

The distribution of anti-spike IgG avidity and anti-nucleocapsid IgG avidity was examined by epidemiologic characteristics, including sex, age, race/ethnicity, and hospitalization status (ie, COVID-19 illness severity). Differences between groups were calculated by Wilcoxon rank-sum tests or Kruskal-Wallis tests, as appropriate. Correlations between age and avidity were assessed by Pearson correlation coefficient. Ordinary least-squares linear regression was used to examine the association of age, sex, and hospitalization status with avidity DC50 values. Multivariable models included age, sex, and hospitalization status regardless of statistical significance, as they have previously been shown to be important for other IgG antibody responses in this study population [19]. The multivariable analysis also included adjustment for time since symptom onset. Subgroup analyses were performed stratified by sex using similar methodology. The primary analysis included avidity DC50 values for individuals who were considered indeterminate for a given IgG ELISA based on the manufacturer’s cutoff. Thus, sensitivity analyses were performed that excluded donors who had an indeterminate sample.

As a secondary analysis, evaluations of whether anti-spike IgG titers and avidity as well as anti-nucleocapsid IgG titers and avidity correlated with NT AUC values. Data were visualized with nonparametric locally weighted scatterplot smoothing (LOWESS) curves and correlations were assessed with Spearman rank correlation coefficients. To determine whether IgG titers and avidity are associated with elevated neutralizing antibodies, modified Poisson regression with robust variance was used to estimate prevalence ratios (PR) and corresponding 95% confidence intervals (CI) of an NT AUC value ≥160. Multivariable analyses were performed including the serologic biomarker of interest, age, sex, hospitalization status, and time since symptom onset. This analysis was also repeated using an NT AUC value ≥40 as the outcome of interest.

Sensitivity analyses were also performed including days since initial positive PCR diagnosis in multivariable models as opposed to self-reported days symptom onset; time since initial positive PCR-positive diagnosis, which was confirmed with medical documentation, may be a more reliable indicator of duration of infection than a self-reported measure.

RESULTS

Characteristics of the Study Population

There were 16 hospitalized COVID-19 patients in the longitudinal cohort who contributed an average of 5 samples per person (n = 84 total samples). Plasma samples were collected from patients at a median of 13 days (range, 4–35; IQR, 10–16) after symptom onset (Table 1). Using the manufacturers’ cutoffs, 76% (n = 64) of the samples were considered seropositive for anti-spike IgG by the Euroimmun assay and 89% (n = 75) were considered seropositive for anti-nucleocapsid IgG using the EDI assay. Of note, 19 (23%) samples were seronegative for anti-spike IgG and 7 (8%) samples were seronegative for anti-nucleocapsid IgG. However, all specimens collected after 14 days since symptom onset were considered to be seropositive by the Euroimmun assay and the EDI assay (Supplementary Table 1). IgG avidity was measured in seropositive and indeterminate specimens; anti-spike IgG avidity was measured in 65 samples (16 patients) and anti-nucleocapsid IgG avidity was measured in 76 samples (16 patients).

Table 1.

Characteristics of Participants Overall and by Sex

Characteristics	No. of Samples (%) (n = 84 Samples; N = 16 Participants)
Longitudinal Cohort
Days post symptom onset (IQR)	13 (10–16)
Euroimmun anti-spike IgG
Seropositive	64 (76)
Indeterminate	1 (1)
Seronegative	19 (23)
EDI anti-nucleocapsid IgG
Seropositive	75 (89)
Indeterminate	2 (2)
Seronegative	7 (8)
Convalescent Plasma Cohort
	No. of participants (%)
	Overall (n = 130)	Female (n = 60)	Male (n = 70)
Age group, y
18–29	34 (26)	17 (28)	17 (24)
30–39	23 (18)	9 (15)	14 (20)
40–49	28 (22)	13 (22)	15 (21)
50–59	23 (18)	11 (18)	12 (17)
≥60	22 (17)	10 (17)	12 (17)
Race/ethnicity
Non-Hispanic white	98 (75)	47 (78)	51 (73)
Non-Hispanic black	4 (3)	2 (3)	2 (3)
Hispanic	5 (4)	4 (7)	1 (1)
Non-Hispanic Asian	14 (11)	2 (3)	12 (17)
Other/multiracial/unknown	9 (7)	5 (8)	4 (6)
Median days post symptom onset (IQR)a	49 (43–55)	50 (43–56)	48 (43–54)
Hospitalization status severity
No	117 (90)	52 (87)	65 (93)
Yes	11 (8)	6 (10)	5 (7)
Missing	2 (2)	2 (3)	0 (0.0)
Euroimmun anti-spike IgG
Seropositive	117 (90)	50 (83)	67 (96)
Indeterminate	7 (5)	5 (8)	2 (3)
Seronegative	5 (4)	4 (7)	1 (1)
Missing	1 (1)	1 (2)	0 (0)
EDI anti-nucleocapsid IgG
Seropositive	105 (81)	46 (77)	59 (84)
Indeterminate	9 (7)	5 (8)	4 (6)
Seronegative	16 (12)	9 (15)	7 (10)

Abbreviations: EDI, Epitope Diagnostics Inc.; IgG, immunoglobulin G; IQR, interquartile range.

aData were missing for 1 participant.

There were 130 participants in the cross-sectional sample of convalescent plasma donors; the median age was 42 years (IQR, 29–55), 46% (n = 60) were female, and 75% (n = 98) were non-Hispanic white (Table 1). Plasma samples were collected from donors a median of 49 days (IQR, 43–55) after symptom onset. Only 11 (8%) donors were previously hospitalized during the course of their infection, although 2 donors were missing data on hospitalization status. Using the manufacturers’ cutoffs, 90% (n = 117) of donors were considered seropositive for anti-spike IgG by the Euroimmun assay, while 81% (n = 105) of donors were considered seropositive for anti-nucleocapsid IgG using the EDI assay. There were some samples that were considered indeterminate for anti-spike IgG serostatus (5% [n = 7]) and anti-nucleocapsid IgG serostatus (7% [n = 9]); plasma from 4 donors were indeterminate by both assays. A greater proportion of donors were seronegative for anti-nucleocapsid IgG (12% [n = 16]) than for anti-spike IgG (4% [n = 5]). Characteristics of donors were similar by sex; however, males were more likely than females to be non-Hispanic Asian (17% vs 3%) and seropositive for anti-spike IgG (96% vs 83%). Prevalence of a high neutralizing titer AUC value greater than 160 was 25% (32/126) overall, 21% (12/58) in females, and 29% (20/68) in males.

Longitudinal Trajectories in SARS-CoV-2 IgG Titers and Avidity Responses

Longitudinal trajectories in SARS-CoV-2 IgG titers and avidity responses were examined by time since symptom onset among the cohort of hospitalized COVID-19 patients (Figure 1). Anti-spike IgG titers increased over days post symptom onset and appeared to peak around day 21 before beginning to plateau (Figure 1A). This same trend was observed with anti-spike IgG avidity (Figure 1B). Similarly, anti-nucleocapsid IgG titers increased with duration of illness, but appeared to peak earlier than anti-spike IgG (around day 15; Figure 1C). However, anti-nucleocapsid IgG avidity followed the same trend as anti-spike IgG avidity and appeared to peak around day 21 (Figure 1D).

Figure 1.

Longitudinal trajectories in anti-spike and anti-nucleocapsid SARS-CoV-2 IgG titers and avidity responses in hospitalized COVID-19 patients by time from symptom onset. Plasma samples taken over course of hospitalization were used to evaluate total antibody titers and antibody avidity (DC50). Each patient is represented by a different color. (A) Anti-spike IgG titers; (B) anti-spike IgG avidity; (C) anti-nucleocapsid titers, and (D) anti-nucleocapsid IgG avidity were measured over days since symptom onset. Antibody avidity is indicated by calculated dissociation constant (DC50) where concentration of urea results in 50% of signal loss. Antibody titers are indicated by semiquantitative arbitrary units (AU) calculated from corrected OD (Euroimmun) or direct ODn values (EDI). Abbreviations: COVID-19, coronavirus disease 2019; EDI, Epitope Diagnostics Inc.; IgG, immunoglobulin G; OD, optical density; ODn, normalized optical density; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Epidemiologic Correlates of SARS-CoV-2 IgG Avidity Among Convalescent Plasma Donors

The distribution of anti-spike IgG avidity was examined by sex, age, race/ethnicity, and hospitalization status among convalescent plasma donors (Figure 2). The median avidity value was 4.12 (IQR, 3.52–4.53) among females and 4.27 (IQR, 3.85–4.68) among males (P = .084; Figure 2A). Age was positively correlated with anti-spike IgG avidity among males (r = 0.316; P = .008) but not among females (r = 0.022; P = .872; Figure 2B). There was no significant difference in anti-spike IgG avidity by race/ethnicity (P = .588; Figure 2C). Donors who were hospitalized during the course of their infection had stronger anti-spike IgG avidity than donors who were not hospitalized (P < .001; Figure 2D). After adjustment for age, hospitalization, and time since symptom onset, males had on average greater anti-spike IgG avidity than females but this association was not statistically significant (βadjusted = .248 [95% CI, −.014 to .510]; Table 2). In multivariable analyses, hospitalization was a consistent predictor of stronger anti-spike IgG avidity overall, among females and males. In contrast, age was significantly associated with anti-spike IgG avidity among males (age per 10 years, βadjusted = .150 [95% CI, .032–.267]) but not among females (βadjusted = .018 [95% CI, −.114 to .150]).

Figure 2.

Anti-spike SARS-CoV-2 IgG avidity responses (DC50) by epidemiologic characteristics among potential COVID-19 convalescent plasma donors. Anti-spike IgG avidity was evaluated compared to (A) sex, (B) age, (C) race/ethnicity, and (D) hospitalization. Red diamonds (A, C, D) indicate the arithmetic mean of avidity DC50 values for a given group and (B) avidity DC50 values are denoted by green triangles for males and grey circles for females. Abbreviations: COVID-19, coronavirus disease 2019; DC50, 50% dissociation constant; IgG, immunoglobulin G; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Table 2.

Epidemiologic Correlates of Anti-spike and Anti-nucleocapsid SARS-CoV-2 IgG Avidity (DC50) Among Potential COVID-19 Convalescent Plasma Donors

	Outcome
	Univariable Models		Multivariable Models
Epidemiologic Characteristic	β (95% CI)	P	β (95% CI)	P
Euroimmun antispike IgG avidity DC  50
Overall population
Age, per 10 y	.096 (.002 to .191)	.046	.091 (.004 to .178)	.040
Male sex	.213 (−.075 to .500)	.146	.248 (−.014 to .510)	.063
Hospitalization	1.257 (.799 to 1.715)	< .001	1.258 (.800 to 1.717)	< .001
Time post symptom onset, per 5 d	.047 (−.031 to .124)	.234	.010 (−.061 to .080)	.790
Female population
Age, per 10 y	.012 (−.134 to .158)	.872	.018 (−.114 to .150)	.783
Hospitalization	1.327 (.693 to 1.962)	< .001	1.224 (.571 to 1.877)	< .001
Time post symptom onset, per 5 d	.122 (.011 to .232)	.031	.075 (−.031 to .181)	.161)
Male population
Age, per 10 y	.169 (.045 to .293)	.008	.150 (.032 to .267)	.013
Hospitalization	1.244 (.574 to 1.915)	< .001	1.180 (.519 to 1.840)	.001
Time post symptom onset, per 5 d	−.020 (−.129 to .089)	.715	4.044 (2.980 to 5.108)	.348
EDI antinucleocapsid IgG avidity DC  50
Overall population
Age, per 10 y	.139 (.032 to .247)	.011	.123 (.017 to .229)	.024
Male sex	−.099 (−.432 to .235)	.558	−.040 (−.361 to .280)	.804
Hospitalization	.606 (.064 to 1.148)	.029	.565 (.016 to 1.113)	.044
Time post symptom onset, per 5 d	.033 (−.055 to .122)	.459	.014 (−.073 to .101)	.755
Female population
Age, per 10 y	.142 (−.000 to .284)	.050	.117 (−.023 to .257)	.099
Hospitalization	.352 (−.316 to 1.020)	.295	.357 (−.327 to 1.041)	.299
Time post symptom onset, per 5 d	.028 (−.087 to .142)	.627	.019 (−.092 to .131)	.731
Male population
Age, per 10 y	.138 (−.024 to .301)	.094	.119 (−.043 to .281)	.146
Hospitalization	.889 (.016 to 1.761)	.046	.796 (−.093 to 1.685)	.078
Time post symptom onset, per 5 d	.035 (−.103 to .174)	.612	.012 (−.125 to .148)	.865

Ordinary least-squares linear regression models were used to examine associations with anti-spike and anti-nucleocapsid IgG avidity DC50 values. The multivariable regression models included all other covariates shown. Separate models were constructed for each outcome and subgroup analyses were performed stratified by sex. Values bolded indicate statistical significance (P < .05).

Abbreviations: CI, confidence interval; COVID-19, coronavirus disease 2019; DC50, 50% dissociation constant; IgG, immunoglobulin G; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

The distribution of anti-nucleocapsid IgG avidity was also examined by sex, age, race/ethnicity, and hospitalization status (Figure 3), with similar findings as anti-spike IgG avidity, except sex did not modify the correlation between age and anti-nucleocapsid IgG avidity (Figure 3B). In multivariable analysis, age was associated with anti-nucleocapsid IgG avidity in the overall model (age per 10 years, βadjusted = .123 [95% CI, .017–.229]), as was hospitalization status (βadjusted = .565 [95% CI, .016–1.113]; Table 2).

Figure 3.

Anti-nucleocapsid SARS-CoV-2 IgG avidity responses (DC50) by epidemiologic characteristics among potential COVID-19 convalescent plasma donors. Anti-nucleocapsid IgG avidity was evaluated compared to (A) sex, (B) age, (C) race/ethnicity, and (D) hospitalization. Blue diamonds (A, C, D) indicate the arithmetic mean of avidity DC50 values for a given group and triangles (B) denote avidity DC50 values for males and circles denote avidity DC50 values for females. Abbreviations: COVID-19, coronavirus disease 2019; EDI, Epitope Diagnostics Inc.; DC50, 50% dissociation constant; IgG, immunoglobulin G; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

In sensitivity analyses excluding indeterminate samples, effect estimates were slightly attenuated but inferences remained similar (Supplementary Tables 2 and 3). Inferences were also similar for time since diagnosis when included in the multivariable models as opposed to time from symptom onset (Supplementary Tables 4 and 5).

Associations Between SARS-CoV-2 IgG Responses and Neutralizing Antibody Titers Among Convalescent Plasma Donors

There was a strong positive correlation between anti-spike IgG titers and anti-spike IgG avidity (Spearman ρ = 0.541; P < .001); however, there was no significant correlation between anti-nucleocapsid IgG titers and anti-nucleocapsid IgG avidity (Spearman ρ = 0.165; P = .078; Supplementary Figure 2). Both anti-spike IgG titers and anti-spike IgG avidity were positively correlated with neutralizing antibody titer AUC values (Spearman ρ = 0.772 and 0.386, respectively; P < .001 for both comparisons; Figure 4A and 4B). Higher levels of anti-spike IgG titers (PR = 1.57 [95% CI, 1.42–1.74]) and higher levels of anti-spike IgG avidity (PR = 1.80 [95% CI, 1.45–2.22]) were significantly associated with a higher prevalence of a neutralizing antibody titer AUC value > 160 (Table 3). These associations were also significant after adjustment for age, sex, hospitalization status, and time from symptom onset in multivariable analysis. Similar results were obtained when days since diagnosis was incorporated into the model rather than time from symptom onset (Supplementary Table 6).

Table 3.

Associations Between SARS-CoV-2 IgG Antibody Responses and Elevated SARS-CoV-2 Neutralizing Antibody Titers

	Outcome
	Univariable Models		Multivariable Models
Serologic Biomarker	PR (95% CI)	P Value	aPR (95% CI)	P Value
Neutralizing Antibody Titer AUC value ≥ 160
Anti-spike IgG titers, AU	1.57 (1.42–1.74)	< .001	1.61 (1.43–1.81)	< .001
Anti-spike IgG avidity, DC50	1.80 (1.45–2.22)	< .001	1.58 (1.19–2.12)	.002
log2 anti-nucleocapsid IgG titer, ODn	7.02 (3.64–13.56)	< .001	10.43 (4.65–23.41)	< .001
log2 anti-nucleocapsid IgG avidity, DC50	2.80 (.73–10.75)	.133	1.57 (.40–6.18)	.516
Neutralizing Antibody Titer AUC value ≥ 40
Anti-spike IgG titers, AU	1.24 (1.17–1.31)	< .001	1.24 (1.15–1.33)	< .001
Anti-spike IgG avidity, DC50	1.31 (1.16–1.48)	< .001	1.18 (.99–1.41)	.064
log2 anti-nucleocapsid IgG titer, ODn	2.01 (1.56–2.49)	< .001	2.25 (1.66–3.04)	< .001
log2 anti-nucleocapsid IgG avidity, DC50	1.67 (.84–3.32)	.140	1.42 (.77–2.64)	.264

Prevalence ratios of a neutralizing titer AUC value ≥160 and ≥40 were estimated from Poisson regression models with robust standard errors. A different model was used for each serologic biomarker shown. Multivariable models were used to estimate adjusted prevalence ratios which included adjustment for age, sex, hospitalization, and time from symptom onset. Values bolded indicate statistical significance (P < .05).

Abbreviations: aPR, adjusted prevalence ratio; AU, arbitrary unit; AUC, area under curve; CI, confidence interval; DC50, 50% dissociation constant; ODn, normalized optical density; PR, prevalence ratio.

While there was a strong positive correlation between anti-nucleocapsid IgG titers and neutralizing antibody titer AUC values (Spearman ρ = 0.685; P < .001; Figure 4C), the correlation between anti-nucleocapsid IgG avidity and neutralizing antibody titer AUC values was weak (Spearman ρ = 0.211; P = .026) and nonlinear (Figure 4D). Anti-nucleocapsid IgG titers were strongly associated with a higher prevalence of a neutralizing antibody titer AUC value ≥160 in univariable, as well as multivariable analysis (Table 3). Anti-nucleocapsid IgG avidity did not have a statistically significant association with neutralizing antibody titer AUC value ≥160 (adjusted PR = 1.57 [95% CI, .40–6.18]). Associations were attenuated when considering a neutralizing antibody titer AUC value ≥40 but remained in the same direction of association.

Figure 4.

Correlations of anti-spike and anti-nucleocapsid SARS-CoV-2 IgG responses with neutralizing antibody titers among potential COVID-19 convalescent plasma donors. Correlations between neutralizing antibody titer AUC values and (A) anti-spike IgG titers, (B) anti-spike IgG avidity, (C) anti-nucleocapsid IgG titers, and (D) anti-nucleocapsid avidity were examined using Spearman correlation coefficient and nonparametric LOWESS curves. Antibody avidity is indicated by calculated dissociation constant (DC50) where concentration of urea results in 50% of signal loss. Antibody titers are indicated by arbitrary units (AU) calculated from corrected OD (Euroimmun) or direct ODn values (EDI). Abbreviations: AUC, area under the curve; COVID-19, coronavirus disease 2019; EDI, Epitope Diagnostics Inc.; IgG, immunoglobulin G; ODn, normalized optical density; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

DISCUSSION

SARS-CoV-2 remains a critical health threat. Better understanding of antibody development is necessary. While antibody response is used to evaluate both the early and late stages of immune responses, the relationship between antibody titers and avidity has yet to be established in COVID-19 [22, 23]. Antibody avidity testing has been used to aid in diagnosis of recent infections, including Epstein-Barr virus, HIV, West Nile Virus, and other SARS CoV infections [24-27]. As some recovered patients do not develop high antibody titers following infection, not everyone is an ideal candidate for plasma donation and those who are may find it burdensome to return to the clinic following titer testing to donate plasma. Thus, based on these data that anti-spike IgG avidity is better correlated with neutralizing titers, testing antibody avidity has potential use as another screening parameter to identify optimal convalescent plasma donors. However, further research is needed to examine the potential benefit of this strategy.

As was expected, antibody avidity and titers were low during initial infection, but increased as infection progressed. In previous SARS outbreaks, low antibody avidity was observed early in infection and increased within the first month of symptom onset [22, 23]. Additionally, high IgG avidity was observed 3 weeks following symptom onset in recovered COVID-19 individuals [28]. Consistent with those findings, anti-spike and anti-nucleocapsid IgG avidity increased with antibody titers within the first month of symptom onset and remained elevated following viral clearance. Of the 2 major immunogenic proteins, nucleocapsid proteins are more abundantly expressed, which could help to explain why titers for anti-nucleocapsid IgG appears earlier than anti-spike IgG [22, 29]. Avidity for both antibodies appears to peak around 3 weeks following symptom onset, which corresponds to previous reports of IgG seroconversion in COVID-19 patients occurring between 8 and 21 days following symptom onset [30, 31].

Male bias has been documented in COVID-19 patients, with males having increased disease severity and mortality compared to females [32-34]. Additionally, increased risk for severity of disease is associated with advancing age, even though males and females both have the same susceptibility risk [33, 35]. In the convalescent plasma cohort, antibody avidity was increased in older males compared to younger males. However, no statistically significant differences in anti-spike or anti-nucleocapsid avidity between males and females was observed, which may potentially be due to lack of power, particularly for anti-spike avidity. All participants donating convalescent plasma had recovered from COVID-19, and even though males tend to have a higher mortality rate than females, those parameters were not established in these studies.

Avidity was significantly higher among hospitalized patients compared to those who were not hospitalized. Those hospitalized may have had higher viral loads and/or increased exposure, exacerbating symptoms, increasing immune response and antibody production to combat increased viral loads. Moreover, anti-spike avidity was correlated with higher neutralizing antibody titers. Neutralizing antibodies prevent viral replication by binding to viral proteins and blocking the interaction with cellular receptors or cell surface attachment to inhibit host membrane fusion [36]. There was a correlation between anti-nucleocapsid titers and neutralizing antibody titer AUC, but this may reflect the overall anti-SARS-CoV-2 antibody levels, as anti-nucleocapsid antibodies are not believed to have neutralizing activity. However, nucleocapsid antibodies may be necessary for viral clearance via antibody-dependent cellular cytotoxicity, antibody-dependent cell-mediated phagocytosis, and/or complement activation [33, 35].

Asymptomatic individuals have lower antibody titers as compared to symptomatic patients and those individuals who recover from COVID-19 without becoming hospitalized typically do not have high neutralizing antibody activity [36]. In these studies, persons infected with SARS-CoV-2 who were symptomatic but not hospitalized had lower antibody avidity and 4%–12% had no detectable antibody titers. Those with low titers and avidity may have either robust innate immune or adaptive T-cell responses or strongly binding antibodies early during exposure that results in viral clearance, and it will be important to examine these additional aspects of the anti-COVID immune response moving forward. The mechanisms behind why some individuals do not reach detectable antibody titers following viral clearance needs further investigation.

This study had limitations. Antibody titers were analyzed using 2 different methods, and although increasing values of AU and/or ODn may indicate increase in antibody titers, these values are proxies for quantitative measures. Plateaus observed in both assays may be due, in part, to a small dynamic range of the assay, and as a result antibodies do not appear to continue to rise. Only hospitalized patients were assessed in the longitudinal study and the antibody titers or avidity findings may not be generalizable to those who have mild or subclinical disease. Longitudinal samples did not have demographic characteristics collected, so avidity cannot be attributed to sex or age differences in that cohort. In the convalescent plasma donors, less than 10% were hospitalized and only 1 time point was collected per individual.

Additionally, the usage of modified ELISA avidity assays have not been approved by the FDA for convalescent plasma qualification. However, alternative antibody assays are under evaluation for convalescent plasma testing [37]. Although this study did not analyze longitudinal convalescent plasma, it should be further investigated as reports of declining antibody titers are observed 2–3 months following infection [38]. This would help to identify the optimal window of plasma donation. Furthermore, future studies should explore convalescent plasma in relation to ABO blood groups [39, 40].

The use of avidity in conjunction with other serologic testing may be useful in establishing parameters for optimal convalescent plasma donor screening. Increase in avidity following viral clearance is a good indication that strong antibodies and/or neutralizing antibodies are still present. Those with higher anti-spike antibody avidity also have higher neutralizing titers and can aid in identification of those who establish robust adaptive immune response to infection.

Supplementary Data

Supplementary materials are available at The Journal of Infectious Diseases online. Consisting of data provided by the authors to benefit the reader, the posted materials are not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author.

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