key: cord-1047804-b1niptp8
authors: Eichholz, Thomas; Arendt, Anne-Marie; Holzer, Ursula; Seitz, Christian; Rabsteyn, Armin; Ganzenmueller, Tina; Klein, Reinhild; Walz, Juliane; Lang, Peter
title: Recurrent SARS-CoV-2 Infection and Impaired Immunologic Response in a Pediatric Oncologic Patient While Treated With Radiochemotherapy
date: 2022-05-06
journal: Pediatr Infect Dis J
DOI: 10.1097/inf.0000000000003515
sha: d832feff3821e54e346f16b770b07783fda24db4
doc_id: 1047804
cord_uid: b1niptp8

Immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in pediatric patients with malignant disease may be affected by tumor therapy. Here, we report the case of a child with rhabdomyosarcoma and recurrent SARS-CoV-2 infection. Immunologic responses, analyzed by T-cell activity and anti-viral IgG levels, were impaired and not durable as a result of intensive radiochemotherapy.

T he severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has caused substantial morbidity and mortality. The impact of SARS-CoV-2 infection in children is an ongoing matter of discussion, as children appear to be infected less commonly and with a milder course of the disease. 1 However, the rate of infection is likely to be underestimated because infections in children are often asymptomatic and are therefore tested less frequently. Throughout the pandemic, severe courses of the primary disease as well as pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 have been observed in children. Increased symptomatic infections were observed as the coronavirus evolved, including variants B1.1.7 2 and B1.617.2. 3 Although children with underlying malignant disease are usually at a higher risk for infections in general, only a few coronavirus disease 2019 cases have been reported during the first wave of the pandemic. 4 Nevertheless, these children are generally classified as high risk. Apart from SARS-CoV-2 associated complications, they may also be affected by a delay in tumor therapy and increased exposure to pathogens within hospital facilities. 5 Furthermore, the ability of these children to develop an adequate immune response is not entirely understood.

To assess T-cell responses against SARS-CoV-2, patient's peripheral blood mononuclear cells were incubated with SARS-CoV-2-specific peptide mixes (SI and SII, containing human leukocyte antigen class I and II SARS-CoV-2-exclusive T-cell epitopes) and cross-reactive peptide mixes (CI and CII, containing human leukocyte antigen class I and II T-cell epitopes derived from conserved sequences of coronavirus antigens). 6 After in vitro peptide stimulation, intracellular cytokine staining was performed to detect antigen-specific T cells as described previously. 6 For the gating strategy for the detection of specific T-cell responses, see Figure  1 (Supplemental Digital Content, http://links.lww.com/INF/E696).

We report the case of an 11-year-old boy with rhabdomyosarcoma and subsequent SARS-CoV-2 reinfection. The patient was diagnosed with disseminated stage IV alveolar rhabdomyosarcoma in November 2019 (day 1). Histology was confirmed by paratesticular biopsy of the suspected primary site. Subsequent radiochemotherapy was initiated according to the Cooperative Weichteilsarkom Study Group guidance. Orchidectomy was performed after neoadjuvant therapy. Following the fifth cycle of polychemotherapy, including ifosfamide, vincristine, actinomycin, carboplatin, epirubicin and etoposide, the patient presented with a globus sensation and subfebrile temperature. There were no additional signs suggestive of SARS-CoV-2 infection, such as respiratory symptoms or an altered sense of smell and taste. SARS-CoV-2-RNA was detected in a pharyngeal swab by real-time polymerase chain reaction (RT-PCR; Ct value of E-gene PCR 32) in April 2020 (day 135) during the first pandemic wave in Germany. Laboratory results showed neutropenia (40/µL), lymphopenia (131/µL) and elevated C-reactive protein (CRP) value (4.82 mg/dL). Lactate dehydrogenase and D-dimer levels were not significantly altered.

The follow-up pharyngeal swab, 1 week after the first SARS-CoV-2 detection, was negative for SARS-CoV-2-RNA, as were consecutive oropharyngeal swabs from days 146 to 261. Three weeks after the first negative RT-PCR and after hematopoietic recovery, Blood samples of our patient were retrospectively analyzed for the immune response towards SARS-CoV-2. At the time of the first SARS-CoV-2 infection, the patient received chemotherapy, resulting in significantly decreased lymphocyte counts (Fig. 1A) .

At time point 1 (day 169), three weeks after clearing the first SARS-CoV-2 infection (Fig. 1D) , only a borderline in vitro CD8+ T-cell response and no CD4+ response were observed against SARS-CoV-2-specific peptides (peptide mixes SI/SII). In contrast, a clear response of CD4+ T cells against cross-reactive peptides (peptide mix CII) was observed (Fig. 1B) . During subsequent intense radiochemotherapy, lymphocyte counts remained low (maximum 580/µL between March and November). However, stimulation of T cells with staphylococcal enterotoxin B, serving as a positive control, resulted in cytokine secretion, indicating a remaining T-cell function (Fig. 1B) . No antibody response was detected under chemotherapy.

In November 2020 (360 days after the initial diagnosis of sarcoma), the patient developed dry cough and headaches. Subsequent testing for SARS-CoV-2 revealed RNA in the pharyngeal swab on days 360 and 369. Next-generation sequencing (Illumina) detected the SARS-CoV-2 lineage B.1.1.70 (Pangolin tool v3.1.11, https://pangolin.cog-uk.io/ and https://pangolin.cog-uk.io/), a strain circulating in Germany that time (GISAID Accession Number EPI_ ISL_4528405). Infection likely occurred after exposure to SARS-CoV-2 positive close family members. In addition to neutropenia and lymphopenia, the patient did not develop fever or significantly altered laboratory results. However, routine magnetic resonance imaging performed to evaluate remission status revealed lung infiltration, possibly attributable to coronavirus disease 2019. In a second swab obtained 1 week later, SARS-CoV-2 RNA was still detectable (Ct value E-gene = 26). Following 2 consecutive negative SARS-CoV-2 swabs (days 376 and 379), subsequent swabs demonstrated faintly positive results (Ct value E-gene >35) on days 387 and 394. All further follow-up swabs (sampled at 16 time points from days 401 to 524) remained negative for SARS-CoV-2 RNA, indicating that SARS-CoV-2 reinfection was cleared. Stool specimens were not analyzed for viral shedding. SARS-CoV-2 antibody ELISA revealed seroconversion with the detection of anti-nucleocapsid IgG. The antibody response occurred with recovery of B-cell counts after completion of intense radiochemotherapy (Fig. 1A) .

At time point 2, 9 weeks after the last positive PCR test, T-cell responses were re-evaluated. Strong CD3+CD4+ and CD3+CD8+ T-cell responses against specific SARS-CoV-2 peptide mixes SI and SII, as well as against cross-reactive peptide mixes CI and CII, were evident (Fig. 1C) .

Despite salvage radiation and intrathecal chemotherapy, the patient died as a result of the underlying oncological disease after experiencing intracranial relapse.

Prolonged virus shedding for more than 100 days, 7 recurrent detection of SARS-CoV-2 RNA, 5 and de novo reinfections 8 have been reported for SARS-CoV-2, especially in immunocompromised patients. Differentiating between persistent shedding and reinfection is a challenging task. In the present case, it is likely that the patient had experienced 2 subsequent SARS-CoV-2 infections. Although sampling at a low viral load during the first episode was insufficient for sequencing, the SARS-CoV-2 lineage was successfully determined for the second episode. Since the detected strain was predominantly circulating during the second wave in Germany (November 2020), a second de novo reinfection is most likely. Additionally, the relatively long interval between April and November, the known infection source (exposure from SARS-CoV-2 positive family members), and typical clinical symptoms including pulmonary infiltration during the second infection 9 argue in favor of a reinfection.

It is likely that the T-cell response at time point 1 reflects preexisting cross-reactive CD4+ T cells originating from previous infections with endemic coronaviruses related to SARS-CoV-2. These T cells represent preformed memory cells that are reactive to peptide sequences included in the cross-reactive peptide mix. The peptide mixtures CI and CII consist of sequences conserved across coronaviruses, SARS-CoV-2 and other endemic coronaviruses. Therefore, a large proportion of the healthy population has memory T cells against these antigens. 6 The cross-reactive cells in the present patient might have been acquired before the first SARS-CoV-2 infection but could also have developed as a result of it. Kundu et al 10 recently showed that such cross-reactive memory T cells are associated with protection against SARS-CoV-2 infection.

Thus, the detected cross-reactive CD4+ and the borderline specific CD8+ response might have contributed to the clearance of the patient's first infection. Antitumor therapy before and after the first infection seemed to hamper the production of specific antibodies, which were not detected by ELISA. The absence of seroconversion is associated with profound therapy-related lymphopenia and B-cell deficiency. Moreover, insufficient T-cell priming and cytokine support may negatively influence seroconversion, antibody production and release.

In contrast, the second infection resulted in strong and persistent CD4+ and CD8+ responses against both cross-reactive and specific peptides, as well as clear seroconversion. At that time point, the intense antitumor therapy was terminated and did not severely interfere with the cellular immune response.

Reinfections with SARS-CoV-2 have also been reported in patients without preexisting oncological conditions, but are still very rare, considering the high number of infections worldwide. 8 The duration of protective immune responses is not clear, since long-term follow-up studies are limited to date, and immunity following the first SARS-CoV-2 infection might be insufficient against emerging virus variants. Nevertheless, the patient experienced a second infection in close temporal proximity to the first infection, which did not result in a sufficient antibody response. Even though the marginal T-cell response appears to be sufficient to clear the virus initially, long-lasting protection was impaired by subsequent therapy. Thus, radiochemotherapy can inhibit a durable immune response and increase the risk of reinfections.

Conversely, cancer patients are not only endangered by the virus but also by a delay in treatment protocols, and mild SARS-CoV-2 symptoms should not necessarily lead to a long-lasting interruption.

Regular screening can help detect reinfections at an early stage and initiate appropriate measures. Since family members are a common source of infection, immunization of caretakers and siblings with priority, according to national approval and guidelines, should be encouraged.

In summary, a limited and transient immune response can occur in children diagnosed with cancer undergoing radiochemotherapy, and previously acquired immunity might be impaired by these therapies.

Systematic review of COVID-19 in children shows milder cases and a better prognosis than adults

SARS-CoV-2 variant B.1.1.7 susceptibility and infectiousness of children and adults deduced from investigations of childcare centre outbreaks

Public Health Scotland and the EAVE II Collaborators. SARS-CoV-2 Delta VOC in Scotland: demographics, risk of hospital admission, and vaccine effectiveness

Management of the COVID-19 outbreak in a pediatric hemato-oncology department Early experience in protecting immunocompromised patients in Lombardia

Prolonged SARS-CoV-2-RNA detection from nasopharyngeal Swabs in an oncologic patient: what impact on cancer treatment?

SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition

Case Study: prolonged infectious SARS-CoV-2 shedding from an asymptomatic immunocompromised individual with cancer

Genomic evidence for reinfection with SARS-CoV-2: a case study

COVID-19 reinfection: prolonged shedding or true reinfection?

Cross-reactive memory T cells associate with protection against SARS-CoV-2 infection in COVID-19 contacts

We thank Silke Peter from the Institute of Medical Microbiology (University Tuebingen) for typing of the SARS-CoV-2 lineage by high-throughput sequencing. The authors acknowledge the