User profiles for Antonio Condino-Neto
Antonio Condino-Neto, MD, PhD, FAAAAIChief Medical Officer - Immunogenic Verified email at immunogenic.com.br Cited by 8443 |
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
Circulating autoantibodies (auto-Abs) neutralizing high concentrations (10 ng/ml; in plasma
diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 …
diluted 1:10) of IFN-α and/or IFN-ω are found in about 10% of patients with critical COVID-19 …
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies
…, C Erikstrup, A Condino-Neto… - Proceedings of the …, 2022 - National Acad Sciences
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection fatality rate (IFR)
doubles with every 5 y of age from childhood onward. Circulating autoantibodies neutralizing …
doubles with every 5 y of age from childhood onward. Circulating autoantibodies neutralizing …
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease
…, B Woda, PE Newburger, A Condino-Neto… - Nature …, 2011 - nature.com
Germline mutations in CYBB, the human gene encoding the gp91 phox subunit of the phagocyte
NADPH oxidase, impair the respiratory burst of all types of phagocytes and result in X-…
NADPH oxidase, impair the respiratory burst of all types of phagocytes and result in X-…
[PDF][PDF] A global effort to define the human genetics of protective immunity to SARS-CoV-2 infection
SARS-CoV-2 infection displays immense inter-individual clinical variability, ranging from silent
infection to lethal disease. The role of human genetics in determining clinical response to …
infection to lethal disease. The role of human genetics in determining clinical response to …
Hematologically important mutations: X-linked chronic granulomatous disease (third update)
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. The disease is caused by a lack of superoxide production by the …
250,000 individuals. The disease is caused by a lack of superoxide production by the …
Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry
…, M Carneiro-Sampaio, A Condino-Neto… - Journal of Clinical …, 2007 - Springer
This is the second report on the continuing efforts of LAGID to increase the recognition and
registration of patients with primary immunodeficiency diseases in 12 Latin American …
registration of patients with primary immunodeficiency diseases in 12 Latin American …
Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant
Inherited IL-12Rβ1 and TYK2 deficiencies impair both IL-12– and IL-23–dependent IFN-γ
immunity and are rare monogenic causes of tuberculosis, each found in less than 1/600,000 …
immunity and are rare monogenic causes of tuberculosis, each found in less than 1/600,000 …
[HTML][HTML] Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency
…, K Capuder, A Condino-Neto… - The Journal of …, 2015 - Am Soc Clin Investig
Patients with mutations of the recombination-activating genes (RAG) present with diverse
clinical phenotypes, including severe combined immune deficiency (SCID), autoimmunity, and …
clinical phenotypes, including severe combined immune deficiency (SCID), autoimmunity, and …
Global systematic review of primary immunodeficiency registries
…, W Al-Herz, AA Bousfiha, A Condino-Neto… - Expert review of …, 2020 - Taylor & Francis
Introduction During the last 4 decades, registration of patients with primary immunodeficiencies
(PID) has played an essential role in different aspects of these diseases worldwide …
(PID) has played an essential role in different aspects of these diseases worldwide …
[HTML][HTML] Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
…, G Casari, K Chaïbi, R Colobran, A Condino-Neto… - Genome medicine, 2023 - Springer
Background We previously reported that impaired type I IFN activity, due to inborn errors of
TLR3- and TLR7-dependent type I interferon (IFN) immunity or to autoantibodies against type …
TLR3- and TLR7-dependent type I interferon (IFN) immunity or to autoantibodies against type …