Journal of Medical Virology | 2021
SARS‐CoV‐2 reinfection in a cancer patient with a defective neutralizing humoral response
Abstract
To the Editor, Since August 2020, a series of cases of reinfection by a phylogenetically distinct variant of SARS‐CoV‐2 have been reported, raising pertinent questions on the heterogeneity of the natural immune response to SARS‐ CoV‐2 infection that may not uniformly confer protective immunity to all individuals. Specifically, reinfection seems more likely to occur in individuals whose immune system has been weakened by underlying comorbidities or therapies. Here, we report a case of a 52‐year‐old male patient suffering from transitional cell carcinoma of the renal pelvis and ureter who was infected at two separate times with two genetically distant SARS‐CoV‐2 strains, with the reappearance of the first strain four months after the first infection. The patient s past medical history and treatments are summarized in Figure S1. On June 23, 2020 (Day 0), he had a cough and fever and was diagnosed with COVID‐19 by SARS‐CoV‐ 2 reverse transcriptase‐polymerase chain reaction (RT‐PCR) assay of a nasopharyngeal swab specimen (cycle threshold, Ct, values for SARS‐ CoV‐2 E, RdRp, and N genes ranged from 25 to 26) (Figure 1A). Chest X‐ray did not reveal any abnormality, and his clinical conditions improved with resolution of cough and fever within 2 weeks. On Days 35 and 36, two consecutive nasopharyngeal swabs resulted negative for SARS‐CoV‐ 2 infection. In the next few months, the patient did not show any respiratory symptoms. However, the deterioration of his cancer condition leading to urinary tract infection and sepsis required further hospitalization. On Day 110, the patient had a fever caused by an ongoing Escherichia coli‐induced sepsis. RT‐PCR assay of a nasopharyngeal swab resulted positive again, causing concern for a recurrence of COVID‐19 (Ct values of 34 and 36 for E and N genes, and over 40 for the RdRp gene). An abdominal computed tomography scan performed on Day 113 showed thrombosis of the inferior vena cava, of the right iliac vein, and of both femoral veins. On Day 115, the patient died from septic shock and respiratory failure. Quantitative SARS‐CoV‐2 viral loads by droplet digital PCR detected 546, 1, and 53 copies/μl on Days 0, 110, and 115 nasopharyngeal swabs, respectively (Figure 1A). Whole‐genome sequencing and phylogenetic analysis of RNA from the first two specimens showed that the viral genome found at Day 0 could be grouped in the Nextstrain clade 20B and Pangolin lineage B.1.1, while the strain isolated on Day 110 belonged to the Nextstrain clade 20A and Pangolin lineage B.1 (Figure 1B). However, when we sequenced the RNA from the third sample harvested on Day 115, we detected again the Nextstrain clade 20B, suggesting that the first infection strain had never been cleared completely. With regard to amino acid changes, by analyzing minority variants in the Day 115 specimen, the mutations R203K and G204R, which distinguish B.1 and B.1.1 lineages, were the predominant ones until 65% coverage, but below this cut‐off, we were also able to detect significant levels of the wild‐type virus (Figure 1C). Furthermore, the D614G variant was always present in specimens isolated on Days 110 and 115, whereas it was absent, even as a minority variant, in the specimen harvested on Day 0. No evidence of recombination events was observed. Phylogenetic analysis was congruent with both persistent infection with B.1.1 strains (specimens from Days 0 and 115) and reinfection with B.1 strain on Day 110. The patient s blood was only available on Day 110 and resulted negative for the presence of SARS‐CoV‐2 genome by droplet digital PCR analysis. Rapid immunochromatographic test on blood resulted positive for immunoglobulin G (IgG) anti‐SARS‐ CoV‐2 N protein. Very low levels of IgG anti‐SARS‐CoV‐2 spike protein were found in this sample (1200 AU/ml with the low threshold < 2.544 AU/ml). In addition, anti‐receptor binding domain antibodies were determined by a different enzyme‐linked immunosorbent assay, which confirmed the presence of very low reactivity. Consistently, the neutralizing activity performed using the replication‐competent chimeric VSV expressing the SARS‐ CoV‐2 spike protein (rVSV‐SARS‐CoV‐2‐SΔ21) was very low when compared to convalescent positive control. The inhibitory concentration (IC50) of the positive control was 0.0007 while the patient s serum was a thousand times less potent (IC50 = 0.1) and barely reached 50% of neutralization at the lowest serum dilution of 1:10 (Figures 1D and S2). The fact that VSV harbors the D614 form of the spike protein—the same found in the strain isolated on Day 0—and that the G614 form is reportedly unable to interfere with the neutralizing titer rules out any detection bias of our approach, indicating that the patient did fail to mount an appropriate neutralizing humoral response. Overall, this case highlights the concerning risk of reinfection in cancer patients who fail to mount an efficient neutralizing humoral response along with the underlying existence of persistent asymptomatic/undetectable infection.