key: cord-0743621-odeeorcj
authors: Inada, Makoto; Ishikane, Masahiro; Terada, Mari; Matsunaga, Akihiro; Maeda, Kenji; Tsuchiya, Kiyoto; Miura, Kenji; Sairenji, Yu; Kinoshita, Noriko; Ujiie, Mugen; Kutsuna, Satoshi; Ishizaka, Yukihito; Mitsuya, Hiroaki; Ohmagari, Norio
title: Asymptomatic COVID-19 Re-infection in a Japanese Male by Elevated Half-Maximal Inhibitory Concentration (IC50) of Neutralizing Antibodies
date: 2021-04-24
journal: J Infect Chemother
DOI: 10.1016/j.jiac.2021.04.017
sha: ce411f095739cd89b36c385c497c86242fbf9a52
doc_id: 743621
cord_uid: odeeorcj

Introduction "Re-infection" with COVID-19 is a growing concern; re-infection cases have reported worldwide. However, the clinical characteristics of SARS-CoV-2 re-infection, including the levels and role of anti-SARS-CoV-2 Spike protein IgG antibodies and the half-maximal concentration (IC50) of neutralizing antibodies remain unknown. Methods Both the epidemiological and clinical information has been collected during two episodes of COVID-19 in a patient. Laboratory results, including RT-PCR, Ct values, anti-SARS-CoV-2 Spike protein IgG antibodies, and the IC50 of neutralizing antibodies levels were analyzed on the patient. Results The patient was a 58-year-old man who developed moderate COVID-19 pneumonia with oxygen demand (cannula 2 L/min) in the first episode. By day 30, he recuperated and was discharged after testing negative for SARS-CoV-2. After two and a half months, his three family members showed COVID-19 symptoms and tested positive for SARS-CoV-2. He tested positive for SARS-CoV-2 once again and was asymptomatic (the second episode). The IC50 of neutralizing antibodies against SARS-CoV-2 greatly increased from 50.0μg/mL (after the first episode) to 14.8 μg/mL (after the second episode), and remained strongly reactive (20.1 μl/mL) after 47 days of the second episode. Conclusions Epidemiological, clinical, and serological analyses confirmed that the patient had re-infection instead of persistent viral shedding from first infection. Our results suggest that SARS-CoV-2 re-infection may manifest as asymptomatic with increased neutralizing antibody levels. Further studies such as the virus characteristics, immunology, and epidemiology on SARS-CoV-2 re-infection are needed.

Since December 2019, the novel coronavirus disease , caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread worldwide; more than 120 million cases including over 2.6 million deaths have been detected [1] .

Over 25 million patients have recovered from COVID-19, but "re-infection" cases are a major concern [2] [3] [4] . As IgG antibody titers and neutralizing activity are elevated initially and decline after 1-2 months of acute infection, re-infection is a theoretical possibility [5, 6] . Although some re-infection cases with differences in viral genome sequences have been reported [2] [3] [4] , the clinical characteristics of SARS-CoV-2 re-infection including the levels and role of anti-Spike protein neutralizing antibodies and the half-maximal concentration (IC 50 ) of neutralizing antibodies remain unknown.

Here, we evaluate the epidemiological, clinical, and serological data from an asymptomatic patient re-infected with SARS-CoV-2 105 days after the first episode.

This study was approved by the ethics committee of the NCGM (approval no: J o u r n a l P r e -p r o o f NCGM-G-003536-03) and was conducted in accordance with the Declaration of Helsinki.

COVID-19 was diagnosed based on SARS-CoV-2 RNA detection in nasopharyngeal swab-samples using qRT-PCR [7] .

Recombinant SARS-CoV-2 Spike protein was prepared from cells transfected with a plasmid bearing the DNA encoding the full-length protein using the Expi293 expression system (Thermo Fisher Scientific, Waltham, MA) [8] . The purified protein was coated onto a MaxiSorp 96-well ELISA plate (Thermo Fisher Scientific) overnight at 4℃.

Coated wells were blocked with 1% BlockAce (KAC, Kyoto, Japan) for 1 h at 37℃ and washed six times with phosphate-buffered saline (PBS). The 1/800-diluted patient serum/plasma samples were added and incubated at 37℃ for 1h. The plate was washed with PBS-T (PBS containing 0.2% Tween 20) and incubated with horseradish peroxidase-conjugated anti-human IgG (GeneTex, Irvine, CA) at 37℃ for 30min. After washing with PBS-T, the captured anti-Spike antibodies were detected with J o u r n a l P r e -p r o o f 3,3′,5,5′-tetramethylbenzidine substrate (Nacalai Tesque, Kyoto, Japan). Finally, absorbance at 450 nm (OD 450 ) was measured using a microplate reader (Bio-Rad, Irvine, CA). Samples from healthy volunteer without SARS-CoV-2 were used as negative controls, whereas those from infected patients with high levels of anti-Spike antibodies were used as positive controls. Each sample was assayed in triplicate. Each antibody titer (OD ratio) was calculated by dividing each sample OD value by the mean plus 6 standard deviation of the negative control OD values.

IgG fractions were obtained from convalescent patients' plasma/serum to detect neutralizing antibodies. We used TMPRSS2-overexpressing VeroE6 (VeroE6 TMPRSS2 ) cells and SARS-CoV-2 05-2N (isolated from a patient with COVID-19-[CoV-05]) treated at the NCGM hospital. IgG fractions were purified using a spin column-based antibody purification kit (Cosmo Bio, Tokyo, Japan) according to the manufacturer's instructions.

For the antiviral assay, VeroE6 TMPRSS2 cells were seeded overnight in 96-well plates (1 × Cell Counting Kit-8 (Dojindo, Kumamoto, Japan).

A 58-year-old Japanese man, with a history of mild dyslipidemia, underwent nasopharyngeal testing for SARS-CoV-2 RNA and presented with fever on April 17, 2020. After two days, qRT-PCR revealed a positive readout (cycle threshold [Ct] values of 18.1), and the patient was hospitalized. He works as a branch manager of a company, and his driver, who drives him to and from the company for one hour one way, was diagnosed with severe COVID-19 a few days before. His daughter who had contact with him developed cough and tested negative for SARS-CoV-2 RNA, whereas his wife was asymptomatic and did not undergo testing. His son had no contact with the patient and did not require testing. Upon admission, his body temperature was 37.5°C. Chest computed tomography showed multiple bilateral patchy ground glass opacities. Blood test results showed C-reactive protein levels of 7.1 mg/dL and leukocyte counts of 3700 cells/μL. On April 21, favipiravir was administered due to high oxygen demand (cannula 2 L/min) to treat moderate COVID-19 pneumonia. His fever broke on April 28. Favipiravir was administered until May 4. On May 17, his symptoms improved, two sequential J o u r n a l P r e -p r o o f nasopharyngeal qRT-PCR tests were negative, and he was discharged. There was no relapse of symptoms after discharge (the first episode).

On July 31, the patient, his wife, and daughter underwent a nasopharyngeal test for SARS-CoV-2 RNA because they had close contact with his son, who was febrile and diagnosed with COVID-19 because of positive result of SARS-CoV-2 antigen test on July 29. qRT-PCR readouts were positive for the patient, his wife, and daughter with Ct values of 37.8, 16.5, and 16.0, respectively. Although the patient was asymptomatic, his wife and daughter had mild fever and dysosmia for several days. They returned home after 10 days of hotel isolation (the second episode) (Figure 1 ).

On July 20, the patient visited our hospital to take screening as a candidate for convalescent plasma donor of COVID-19, and then he received the antibody titer test before the second episode. The anti-SARS-CoV-2 Spike protein IgG antibodies levels on July 20 (94 days after the first episode), August 21 (126 days after the first and 21 days after the second episode), September 16 (152 days after the first and 47 days after the second episode) remained high (OD ratios were 15.6, 13.6, and 11.8, respectively).

Although the IC 50 of neutralizing antibodies on July 20 was high (50 µg/mL), that on J o u r n a l P r e -p r o o f August 21 was lower, suggesting a strong reactivity (14.8 µg/mL), that was maintained on September 16 (20.1 µg/mL) (Figure 1 and Figure 2 ).

We evaluate the results of elevated IC 50 of neutralizing antibodies before and after the second episode of an asymptomatic case of COVID-19 re-infection. In the previously reported cases, two genetically different SARS-CoV-2 strains were responsible for re-infection, as per whole-genome sequencing results [2] [3] [4] . Although we could not isolate the virus, the patient was diagnosed as re-infected for the following reasons. First, the interval between the first and second episodes was 105 days. In a previous case report, a pregnant woman (immunocompromised) showed prolonged SARS-CoV-2 RNA shedding for 104 days [9] . Among most COVID-19 patients, SARS-CoV-2 RNA was reduced to undetectable levels one month after the onset of symptoms [5, 10, 11] .

Concurrently, our patient tested negative for SARS-CoV-2 one month after the onset of symptoms. Second, the patient had close contact with a newly infected family member, and intra-family discrepancy was found in Ct values and clinical symptoms. Third, the IC 50 of neutralizing antibodies declined from weakly reactive; 50 µg/mL (after the first episode) to strongly reactive; 14.8 µg/mL (after the second episode), and at 47 days from J o u r n a l P r e -p r o o f the second episode they remained strongly positive as 20.1 µg/mL (Figure 2 ), despite declined neutralizing antibody levels after 1-2 months of acute infection [3] .

SARS-CoV-2 expresses spike protein on its surface and its receptor binding domain (RBD) attaches to angiotensin converting enzyme 2 (ACE2) of host cell.

Previous report showed spike protein has multiple epitopes including RBD, and some anti-RBD antibodies prevent RBD-ACE2 binding and function as neutralizing antibodies [12] . There is correlation between the overall levels of anti-spike or anti-RBD IgG antibodies and neutralizing activity [13] , while non-anti-spike proteins may have neutralizing activity as shown in SARS-CoV, 2002 [14] . Our study may demonstrate the role of anti-Spike protein and neutralizing antibodies in SARS-CoV-2 re-infection.

Anti-Spike protein IgG was present ~3 months after the first infection, but was weakly reactive. However, at 21 days after re-infection, neutralizing antibody levels increased, suggesting that re-infection induced neutralizing antibody production.

Clinical significance of neutralizing antibodies against SARS-CoV-2 has not been well understood, but our study and several reports may indicate the clinical significance. Regarding first episode of infection, previous reports revealed that anti-spike antibody titers, anti-RBD antibody titer, and neutralizing antibody activities tended to be higher in patients with severe disease than in those with mild or moderate J o u r n a l P r e -p r o o f disease [6, 13, 15] . Although the severity of COVID-19 remains unknown in re-infection cases [2, 16, 17] , this patient was asymptomatic. We think that high levels of neutralizing antibodies may reduce disease onset and severity in reinfection episode. First, SARS-CoV-2 mRNA vaccination successfully induced neutralizing antibody and showed efficacy for protection [18, 19] . Second, an asymptomatic re-infection patient will be rarely diagnosed because such patients do not seek for medical care and diagnostic test.

For these reasons, there may be much more asymptomatic or mild symptomatic re-infection patients like our patient worldwide. This suggests that re-infection episode will be too mild or even asymptomatic to be observed due to neutralizing antibodies and other acquired immune response.

While our patient is not incredibly old, nor does he have the obvious immunodeficiency (only dyslipidemia), there are a few reports suggesting the role of neutralizing antibody in immunocompromised host with persistent COVID-19 [20, 21] .

One is a case of a woman in her 60s with history of non-Hodgkin lymphoma in remission while on maintenance therapy with obinutuzumab, anti-CD20 monoclonal antibody, who has persistent symptoms and positive nasopharyngeal PCR test over 12 weeks, and her IgG antibodies for SARS-CoV-2 were undetectable. The patient's symptoms resolved after convalescent plasma administration [20] . Another report described a case of a man However, increased neutralizing antibody levels suggest re-infection. Despite these limitations, to best our knowledge, this case is the first possible SARS-CoV-2 re-infection case in Japan.

In conclusion, SARS-CoV-2 re-infection may manifest as asymptomatic with increased neutralizing antibody levels. Further studies such as the virus characteristics, immunology, and epidemiology on SARS-CoV-2 re-infection are needed.

NCGM-G-003536-03) and was conducted in accordance with the principles embodied in the Declaration of Helsinki.

All authors declare no conflicts of interest regarding this study. 

Coronavirus disease (COVID-19) Weekly Epidemiological Update and Weekly Operational Update

COVID-19 re-infection by a phylogenetically distinct SARS-coronavirus-2 strain confirmed by whole genome sequencing

Asymptomatic reinfection in two healthcare workers from India with genetically distinct SARS-CoV-2

Symptomatic SARS-CoV-2 reinfection by a phylogenetically distinct strain

Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study

Loss of Anti-SARS-CoV-2 Antibodies in Mild Covid-19

Development of genetic diagnostic methods for novel coronavirus 2019 (nCoV-2019) in Japan

Severe acute respiratory syndrome coronavirus 2-specific antibody responses in coronavirus disease patients

Prolonged detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA in an obstetric patient with antibody seroconversion

Findings from investigation and analysis of re-positive cases Korean Centers for Disease Control & Prevention

Viral load dynamics and disease severity in patients infected with SARS-CoV-2 in Zhejiang province, China

Analysis of a SARS-CoV-2-Infected Individual Reveals Development of Potent Neutralizing Antibodies with Limited Somatic Mutation Immunity

Convergent antibody responses to SARS-CoV-2 in convalescent individuals

Monoclonal antibodies to SARS-associated coronavirus (SARS-CoV): Identification of neutralizing and antibodies reactive to S, N, M and E viral proteins

Evolution of antibody immunity to SARS-CoV-2. Nature

Anti-spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection

COVID-19 reinfection tracker

Safety and Immunogenicity of Two RNA-Based Covid-19 Vaccine Candidates

Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine N

A 63-Year-Old Woman with a History of Non-Hodgkin Lymphoma with Persistent SARS-CoV-2 Infection Who Was Seronegative and Treated with Convalescent Plasma

SARS-CoV-2 evolution during treatment of chronic infection

This study was approved by the ethics committee of the NCGM (approval no: