TY - JOUR
T1 - Host-directed therapies for infectious diseases: current status, recent progress, and future prospects
AU - Zumla, Alimuddin
AU - Rao, Martin
AU - Wallis, Robert S.
AU - Kaufmann, Stefan H. E.
AU - Rustomjee, Roxana
AU - Mwaba, Peter
AU - Vilaplana, Cris
AU - Yeboah-Manu, Dorothy
AU - Chakaya, Jeremiah
AU - Ippolito, Giuseppe
AU - Azhar, Esam
AU - Hoelscher, Michael
AU - Maeurer, Markus
AU - AUTHOR GROUP
AU - Marais, Ben
AU - Talom, J. M.
AU - Tientcheu, L.
AU - Ntoumi, Francine
AU - Koussounda, F. K.
AU - Wejse, Christian
AU - Petersen, Eskild
AU - Andersen, Peter Lawætz
AU - Ruhwald, Morten
AU - Aseffa, Abraham
AU - Bonnet, Maryline
AU - Adegnika, A.
AU - Tientcheu, Leopold
AU - Antonio, Martin
AU - Velavan, Thirumalaisamy P.
AU - Kauffman, Stefan
AU - Gyapong, J.
AU - Ippolito, Guiseppi
AU - Rasolof, Voahangy
AU - Rakotosamimanana, Niaina
AU - Maiga, Almoustapha
AU - Diarra, Bassirou
AU - Macete, Eusebio
AU - Garcia-Basterio, Alberto
AU - Bero, Celso
AU - Grobusch, Martin
AU - van de Werf, Tjip
AU - Oukem, O.
AU - Dyrhol-Riise, A. M.
AU - Bjune, G.
AU - Fylkesnes, Knut
AU - Martins, M. R.
AU - Dieye, Tandakha
AU - Dieye, A.
AU - Dieye, Y.
AU - Garcia-Basteiro, Alberto
AU - Kapata, Nathan
PY - 2016
Y1 - 2016
N2 - Despite extensive global efforts in the fight against killer infectious diseases, they still cause one in four deaths worldwide and are important causes of long-term functional disability arising from tissue damage. The continuing epidemics of tuberculosis, HIV, malaria, and influenza, and the emergence of novel zoonotic pathogens represent major clinical management challenges worldwide. Newer approaches to improving treatment outcomes are needed to reduce the high morbidity and mortality caused by infectious diseases. Recent insights into pathogen-host interactions, pathogenesis, inflammatory pathways, and the host's innate and acquired immune responses are leading to identification and development of a wide range of host-directed therapies with different mechanisms of action. Host-directed therapeutic strategies are now becoming viable adjuncts to standard antimicrobial treatment. Host-directed therapies include commonly used drugs for non-communicable diseases with good safety profiles, immunomodulatory agents, biologics (eg monoclonal antibodies), nutritional products, and cellular therapy using the patient's own immune or bone marrow mesenchymal stromal cells. We discuss clinically relevant examples of progress in identifying host-directed therapies as adjunct treatment options for bacterial, viral, and parasitic infectious diseases
AB - Despite extensive global efforts in the fight against killer infectious diseases, they still cause one in four deaths worldwide and are important causes of long-term functional disability arising from tissue damage. The continuing epidemics of tuberculosis, HIV, malaria, and influenza, and the emergence of novel zoonotic pathogens represent major clinical management challenges worldwide. Newer approaches to improving treatment outcomes are needed to reduce the high morbidity and mortality caused by infectious diseases. Recent insights into pathogen-host interactions, pathogenesis, inflammatory pathways, and the host's innate and acquired immune responses are leading to identification and development of a wide range of host-directed therapies with different mechanisms of action. Host-directed therapeutic strategies are now becoming viable adjuncts to standard antimicrobial treatment. Host-directed therapies include commonly used drugs for non-communicable diseases with good safety profiles, immunomodulatory agents, biologics (eg monoclonal antibodies), nutritional products, and cellular therapy using the patient's own immune or bone marrow mesenchymal stromal cells. We discuss clinically relevant examples of progress in identifying host-directed therapies as adjunct treatment options for bacterial, viral, and parasitic infectious diseases
U2 - https://doi.org/10.1016/S1473-3099(16)00078-5
DO - https://doi.org/10.1016/S1473-3099(16)00078-5
M3 - Review article
C2 - 27036359
SN - 1473-3099
VL - 16
SP - E47-E63
JO - Lancet infectious diseases
JF - Lancet infectious diseases
IS - 4
ER -