# Molecular Characterization of Persistent SARS-CoV-2 Infections in Immunocompromised Patients

**Authors:** Patricia Volkow-Fernández, Marco Villanueva-Reza, Santiago Ávila-Ríos, Enrique Mendoza-Ramírez, América Citlali Vera-Jimenez, Alexandra Martin-Onraet, Beda Islas-Muñoz, Pamela Alatorre-Fernández, Rogelio Pérez-Padilla, Daniel Carpio-Guadarrama, Andrea Cárdenas-Ortega, Víctor Hugo Ahumada-Topete, Clara Espitia, Karen Lizbeth Reyes-Barrera, Edgar Sevilla-Reyes, Joel Armando Vázquez-Pérez

PMC · DOI: 10.3390/v18020189 · Viruses · 2026-01-30

## TL;DR

This study shows that immunocompromised patients can have long-lasting SARS-CoV-2 infections with ongoing viral evolution due to weak immune control.

## Contribution

The study provides evidence of sustained viral evolution in immunocompromised patients through longitudinal genomic analysis.

## Key findings

- Persistent SARS-CoV-2 infections in immunocompromised patients can last up to four years.
- Sequential whole-genome sequencing revealed accumulation of non-synonymous mutations in multiple viral genes.
- Viral replication and diversification occur in the absence of effective immune control.

## Abstract

Immunocompromised patients, including those with advanced HIV infection, hematologic malignancies treated with anti-CD20 monoclonal antibodies, or combined immunodeficiencies, are at increased risk of persistent SARS-CoV-2 infection. While long-term viral shedding has been described in these patients, the extent and nature of intra-host viral evolution during long-term infection remain insufficiently documented. In this study, we report longitudinal genomic analyses of SARS-CoV-2 from three immunocompromised individuals with persistent COVID-19: (i) a female patient with follicular lymphoma receiving bendamustine-rituximab therapy with 9 months of persistence, (ii) a male patient with advanced HIV infection following prolonged antiretroviral therapy interruption with 10 months of persistence, and (iii) a female patient with Good’s Syndrome characterized by combined humoral and cellular immune deficiency with apparently four years of persistence. Replication-competent virus was detected over extended periods. Sequential whole-genome sequencing revealed the gradual accumulation of non-synonymous mutations across multiple viral genes, consistent with ongoing viral replication and intra-host diversification in the absence of effective immune control. Although based on a limited number of cases, these findings provide descriptive evidence that persistent SARS-CoV-2 infection in immunocompromised hosts can be associated with sustained viral evolution. This work highlights the importance of continued virological monitoring in selected patients with prolonged infection and contributes to the understanding of SARS-CoV-2 dynamics in settings of impaired immunity.

## Linked entities

- **Proteins:** MS4A1 (membrane spanning 4-domains A1)
- **Chemicals:** bendamustine (PubChem CID 65628)
- **Diseases:** HIV infection (MONDO:0005109), follicular lymphoma (MONDO:0018906), SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** ORF1ab (ORF1a polyprotein;ORF1ab polyprotein) [NCBI Gene 43740578], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, VTN (vitronectin) [NCBI Gene 7448] {aka V75, VN, VNT}, TFPI (tissue factor pathway inhibitor) [NCBI Gene 7035] {aka EPI, LACI, TFI, TFPI1}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** follicular lymphoma (MESH:D008224), Persistent (MESH:D000088562), dysphagia (MESH:D003680), vascular thrombosis (MESH:D013927), respiratory symptoms (MESH:D012818), rheumatoid arthritis (MESH:D001172), death (MESH:D003643), immunodeficiencies (MESH:D007153), sore throat (MESH:D010612), malnutrition (MESH:D044342), bronchiectasis (MESH:D001987), infected (MESH:D007239), COVID (MESH:D000086382), immune deficiency (MESH:D007154), weight loss (MESH:D015431), cough (MESH:D003371), lymphoma (MESH:D008223), humoral and cellular immune deficiency (MESH:C567115), B-cell dysfunction (MESH:D016393), organ damage (MESH:D000092124), interstitial lung disease (MESH:D017563), Thymoma (MESH:D013945), mediastinal mass (MESH:D008477), -cell function impairment (MESH:D006528), multiple sclerosis (MESH:D009103), HIV (MESH:D015658), oncological (MESH:D000072716), prolonged COVID disease (MESH:D008133), MAC (MESH:D015270), Infectious (MESH:D003141), Persistent COVID-19 (MESH:D000094024), headache (MESH:D006261), injury to (MESH:D014947), fibrosis (MESH:D005355), visual loss (MESH:D014786), upper and lower respiratory tract disease (MESH:D012140), impaired immunity (MESH:D020274), Goods syndrome (MESH:D013577), dyspnea (MESH:D004417), Good's Syndrome (MESH:D005359), opportunistic infections (MESH:D009894), chronic kidney disease (MESH:D051436), respiratory insufficiency (MESH:D012131), CMV (MESH:D003586), autoimmune diseases (MESH:D001327), hypogammaglobulinemia (MESH:D000361), pneumonia (MESH:D011014), diarrhea (MESH:D003967), primary or secondary immunodeficiencies (MESH:D000081207), hematologic malignancies (MESH:D019337), hypoxemia (MESH:D000860)
- **Chemicals:** CHOP (-), ensitrelvir (MESH:C000722354), S (MESH:D013455), valganciclovir (MESH:D000077562), dexamethasone (MESH:D003907), rituximab (MESH:D000069283), amino acid (MESH:D000596), bendamustine (MESH:D000069461), Nirmatrelvir Ritonavir (MESH:C000719967), oxygen (MESH:D010100), ivermectin (MESH:D007559), tenofovir alafenamide (MESH:C442442), bictegravir (MESH:C000620396), remdesivir (MESH:C000606551), Dolutegravir (MESH:C562325)
- **Species:** Klebsiella oxytoca (species) [taxon 571], Homo sapiens (human, species) [taxon 9606], Ebola virus (no rank) [taxon 1570291], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Human immunodeficiency virus 1 (no rank) [taxon 11676]
- **Mutations:** H681Y, L452R, T95I, D1146N, H125Y, K77E, R493Q, R158K, H42Y, E484K, A38S, V615A, P681H, Q836R, R115C, 136-144 del, Q183E, C 142-144 del, G446S, L841R, T4175I, P1548L, H69, T4161I, S2103F, H2357Y, V3917G, D936Y, R3802H, F486L, V3349F, A520V, G213E, S197N, F490L, E484A, H69D, R403K, R13L, A484K, Q992H, L2146F, D215G, R346T, V642G, P621S, A484K, E484T, N501Y
- **Cell lines:** Vero E6 — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0574)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944910/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944910/full.md

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Source: https://tomesphere.com/paper/PMC12944910