Immunogenicity and safety of tixagevimab-cilgavimab for COVID-19 pre-exposure prophylaxis in immunocompromised 20 to <40 kg children and adolescents: A pilot, prospective, open-labeled study DOI Creative Commons
Jassada Buaboonnam, Supattra Rungmaitree, Nuntawan Piyaphanee

и другие.

Human Vaccines & Immunotherapeutics, Год журнала: 2024, Номер 20(1)

Опубликована: Ноя. 22, 2024

We evaluated the immunogenicity of 300 mg Tixagevimab-Cilgavimab in immunocompromised children and adolescents who weighed 20 to >40 kg. Six 18-year-old participants were divided into two groups by body weight received (20 <40 kg) 600 (≥40 Tixagevimab-Cilgavimab, respectively. Anti-SARS-CoV-2 receptor-binding domain IgG concentrations pseudovirus neutralizing antibody (NAb) titers measured at 4, 12, 24 weeks after administration compared with reference data from healthy Thai 2 three BNT162b2 vaccinations. Of 59 participants, 49.2% female, a median (IQR) age 12 (9, 15) years; 16 (27.1%) had cancer. NAb (95% CI) for ancestral Wuhan strain comparatively high both dosing regimens (16363.2 [13765.9, 19450.5] vs 17768.3 [15539.5, 20316.9] kg ≥40 respectively) significantly higher than (P < 0.001 both). Omicron BA.4/5 on par regimens. Adverse events mild, well tolerated, slightly more prevalent full-dose Tixagevimab-Cilgavimab. Minimal waning anti-RBD concentrations, comparable reference, was observed concluded that half-dose generated equivalent antibodies standard doses three-dose vaccination. Further study monoclonal long-acting larger cohorts <6-year-old are warranted.

Язык: Английский

From Detection to Protection: Antibodies and Their Crucial Role in Diagnosing and Combatting SARS-CoV-2 DOI Creative Commons
Anoop Kumar, Prajna Tripathi, Prashant Kumar

и другие.

Vaccines, Год журнала: 2024, Номер 12(5), С. 459 - 459

Опубликована: Апрель 25, 2024

Understanding the antibody response to SARS-CoV-2, virus responsible for COVID-19, is crucial comprehending disease progression and significance of vaccine therapeutic development. The emergence highly contagious variants poses a significant challenge humoral immunity, underscoring necessity grasping intricacies specific antibodies. This review emphasizes pivotal role antibodies in shaping immune responses their implications diagnosing, preventing, treating SARS-CoV-2 infection. It delves into kinetics characteristics explores current antibody-based diagnostics, discussing strengths, clinical utility, limitations. Furthermore, we underscore potential SARS-CoV-2-specific antibodies, various therapies such as monoclonal polyclonal anti-cytokines, convalescent plasma, hyperimmunoglobulin-based therapies. Moreover, offer insights vaccines, emphasizing neutralizing order confer immunity along with emerging concern (VOCs) circulating Omicron subvariants. We also highlight challenges field, risks antibody-dependent enhancement (ADE) shed light on associated original antigenic sin (OAS) effect long COVID. Overall, this intends provide valuable insights, which are advancing sensitive diagnostic tools, identifying efficient therapeutics, developing effective vaccines combat evolving threat global scale.

Язык: Английский

Процитировано

5

Receptor Binding for the Entry Mechanisms of SARS-CoV-2: Insights from the Original Strain and Emerging Variants DOI Creative Commons
Mohamed Mahdi,

Irene Wanjiru Kiarie,

János András Mótyán

и другие.

Viruses, Год журнала: 2025, Номер 17(5), С. 691 - 691

Опубликована: Май 10, 2025

Since its emergence in late 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has continuously evolved, giving rise to multiple variants that have significantly altered the trajectory of COVID-19 pandemic. These resulted waves pandemic, exhibiting characteristic mutations spike (S) protein may affected receptor interaction, tissue tropism, and cell entry mechanisms. While virus was shown primarily utilize angiotensin-converting enzyme (ACE2) host proteases such as transmembrane serine protease (TMPRSS2) for into cells, alterations S changes binding affinity use alternative receptors, potentially expanding virus's ability infect different types or tissues, contributing shifts clinical presentation. been linked variations disease severity, new manifestations, transmission dynamics. In this paper, we overview evolving utilization strategies SARS-CoV-2, focusing on how influenced viral mechanisms outcomes across ongoing pandemic waves.

Язык: Английский

Процитировано

0

Clinical characteristics and COVID-19-related outcomes of immunocompromised patients receiving tixagevimab/cilgavimab pre-exposure prophylaxis in Japan DOI Creative Commons
Toshibumi Taniguchi,

Tomoyuki Homma,

Yoichi Tamai

и другие.

Journal of Infection and Chemotherapy, Год журнала: 2024, Номер 31(1), С. 102467 - 102467

Опубликована: Июль 9, 2024

Язык: Английский

Процитировано

0

Immunogenicity and safety of tixagevimab-cilgavimab for COVID-19 pre-exposure prophylaxis in immunocompromised 20 to <40 kg children and adolescents: A pilot, prospective, open-labeled study DOI Creative Commons
Jassada Buaboonnam, Supattra Rungmaitree, Nuntawan Piyaphanee

и другие.

Human Vaccines & Immunotherapeutics, Год журнала: 2024, Номер 20(1)

Опубликована: Ноя. 22, 2024

We evaluated the immunogenicity of 300 mg Tixagevimab-Cilgavimab in immunocompromised children and adolescents who weighed 20 to >40 kg. Six 18-year-old participants were divided into two groups by body weight received (20 <40 kg) 600 (≥40 Tixagevimab-Cilgavimab, respectively. Anti-SARS-CoV-2 receptor-binding domain IgG concentrations pseudovirus neutralizing antibody (NAb) titers measured at 4, 12, 24 weeks after administration compared with reference data from healthy Thai 2 three BNT162b2 vaccinations. Of 59 participants, 49.2% female, a median (IQR) age 12 (9, 15) years; 16 (27.1%) had cancer. NAb (95% CI) for ancestral Wuhan strain comparatively high both dosing regimens (16363.2 [13765.9, 19450.5] vs 17768.3 [15539.5, 20316.9] kg ≥40 respectively) significantly higher than (P < 0.001 both). Omicron BA.4/5 on par regimens. Adverse events mild, well tolerated, slightly more prevalent full-dose Tixagevimab-Cilgavimab. Minimal waning anti-RBD concentrations, comparable reference, was observed concluded that half-dose generated equivalent antibodies standard doses three-dose vaccination. Further study monoclonal long-acting larger cohorts <6-year-old are warranted.

Язык: Английский

Процитировано

0