The Shifting Paradigm of Monoclonal Antibodies in COVID-19 Management: From Early Triumphs to Viral Resistance and Future Perspectives.

Publication date: Jun 11, 2026

Monoclonal antibodies (mAbs) initially played a major role in outpatient COVID-19 management by providing rapid passive immunity and reducing progression to severe disease. However, continuous SARS-CoV-2 evolution progressively compromised the effectiveness of several anti-spike products. This narrative review summarizes the trajectory of COVID-19 mAbs across three phases: early clinical efficacy, loss of efficacy due to immune escape, and future directions. We conducted a narrative review focusing on mechanisms of action, pivotal clinical trials, and real-world effectiveness of neutralizing anti-spike mAbs and host-directed immunomodulatory mAbs. Emphasis was placed on the impact of variants-especially Omicron-on susceptibility and clinical use, as well as on emerging next-generation platforms. First-generation neutralizing mAbs substantially reduced the hospitalization rates during the Alpha and Delta waves, while immunomodulatory mAbs became standard options for the hyperinflammatory phase in hospitalized patients. With the emergence of Omicron and its sub-lineages, extensive immune escape led to marked reductions in neutralization for many earlier anti-spike agents and consequent restrictions in use. Later-generation approaches targeting more conserved epitopes provided temporary solutions but were also challenged by ongoing antigenic drift. Host-directed immunomodulators retained clinical relevance because their mechanism is independent of viral spike mutations. The clinical role of monoclonal antibodies in COVID-19 has been dynamic and increasingly constrained by viral evolution. Future strategies should prioritize broadly neutralizing antibodies targeting conserved epitopes, innovative delivery platforms, and integration with real-time surveillance to preserve clinical utility in the endemic phase and improve preparedness for future outbreaks.

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Concepts Keywords
Basel antimicrobial stewardship
Future COVID-19
Immunomodulatory hospital pharmacy
Outpatient immune escape
Viral monoclonal antibodies
Omicron
SARS-CoV-2
spike protein
tocilizumab

Semantics

Type Source Name
disease MESH COVID-19
drug DRUGBANK Coenzyme M
drug DRUGBANK Tocilizumab
disease MESH Severe Acute Respiratory Syndrome
disease MESH asymptomatic infection
disease MESH dis
disease MESH syndrome
disease MESH thromboinflammation
disease MESH death
disease MESH infection
drug DRUGBANK Spinosad
drug DRUGBANK Angiotensin II
drug DRUGBANK Serine
disease MESH ADCC
pathway KEGG Viral replication
disease MESH cytokine storm
disease MESH hypoxemia
disease MESH CAP
drug DRUGBANK Sarilumab
drug DRUGBANK Indoleacetic acid
disease MESH strain
drug DRUGBANK Trestolone
disease MESH hematologic malignancies
disease MESH inflammation
disease MESH critically ill
drug DRUGBANK Dexamethasone
disease MESH Long COVID
disease MESH fatigue
disease MESH symptom exacerbation
disease MESH brain fog
disease MESH dysautonomia
disease MESH postural orthostatic tachycardia syndrome
disease MESH chest pain
disease MESH injury
disease MESH acute disease
drug DRUGBANK Calcitonin gene-related peptide
disease MESH migraine
disease MESH co infection
disease MESH Acute Respiratory Distress Syndrome
disease MESH Myalgic Encephalomyelitis
drug DRUGBANK (S)-Des-Me-Ampa
disease MESH Pneumonia
disease MESH Park
disease MESH Thrombosis
drug DRUGBANK Ribostamycin
drug DRUGBANK Motavizumab
drug DRUGBANK Guanosine
drug DRUGBANK Diethylpropion

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