«Development Trends
for Human Monoclonal Antibody Therapeutics,» by Aaron L. Nelson, Eugen Dhimolea and Janice M. Reichert, Nature Reviews Drug Discovery, October 2010.
Not exact matches
Weiner, Elliott and colleagues studied the DNA sequences
for two
human monoclonal antibodies — one able to broadly target influenza A viruses and one able to broadly target influenza B viruses — with collaborators at Inovio and MedImmune.
«This panel of neutralizing
antibodies offers the possibility of developing
human monoclonal antibody - based immunotherapy, especially
for health care workers,» noted the authors.
She helped lead a GSK project focused on designing a
monoclonal antibody to link to the HER3 receptor on
human cells as a treatment
for cancer.
To avoid these problems, researchers have been trying to perfect and speed up procedures
for extracting
monoclonal antibodies from
humans, replicating them in a lab, and then injecting them into victims suffering from the diseases they were formed to fight.
Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, called the new work a «significant advance,» noting in a statement that it «opens the way to producing [
monoclonal antibodies] that potentially could be used diagnostically or therapeutically»
for the flu as well as other infectious diseases such as hepatitis C and the
human immunodeficiency virus (HIV), which can lead to full - blown AIDS.
This research has important implications
for the use of DNA - encoded
monoclonal antibody technology as a platform
for delivering the next generation of immunotherapies
for cancer and many
human diseases.
Thus, this study has implications
for analysis of
human vaccine studies, as in addition to searching
for defined lineages it is worthwhile to perform functional analysis of
monoclonal antibodies that may have found new structural solutions to high affinity binding which can not be discerned from DNA sequence alone.
Guselkumab, a fully
human monoclonal antibody targeting IL - 23, in this Phase 2 study
for the treatment of PsA, was well tolerated with no unexpected safety findings in this patient population.2 Guselkumab is now being pursued in a Phase 3 development programme
for psoriatic arthritis.
«The remarkable advance in technologies to isolate and manufacture
human monoclonal antibodies in concentrations high enough to potentially prevent HIV is a major advance and provides the underlying principle
for our enthusiasm
for these trials.»
Fast - MAb addresses the urgent need
for monoclonal antibodies with unprecedented specificity to native
human proteins with delivery in 8 weeks.
Cells were first probed with a primary mouse
monoclonal antibody against
human HMOX1 (Abcam) diluted in PBS containing 1 % BSA, 0.01 % Triton X-100
for 1 hour, washed twice, and then probed with a secondary goat anti-mouse Alexa 488
antibody (Invitrogen)
for 1 hour.
A fully
human, well tolerated
monoclonal antibody, if formulated
for long duration may be a very attractive alternative to daily PrEP oral treatment
for some individuals.
Some of the important and pioneering work
for which Cambridge is best known and which has led to major improvements in people's lives was only possible using animals, from the development of IVF techniques through to
human monoclonal antibodies.
There will be an ongoing need
for a
human post exposure therapeutic and so we're continuing our work with the
human monoclonal antibody as a treatment that can be given to people who are exposed to Hendra virus.
Though
monoclonal antibodies were a model product in his 18 years CMO experience, process development was also performed
for enzymes, hormones, blood factors, immuno - modulants and vaccines with different expression systems such as hybridoma, myeloma, CHO, BHK, insect - cell / baculovirus, adherent animal and
human cells.
These same challenges exist
for human allergy suffers, but recently there has been a major breakthrough in the development of a new, safe and effective therapy using a
monoclonal antibody that specifically binds and neutralizes
human IgE that is responsible
for activating inflammation - producing cells.
Key Highlight: • Facilitated the introduction of HUMIRA (adalimumab)
for the healthcare professionals as the latest and the only fully
human monoclonal antibody against TNF
for the treatment of moderate to severe psoriasis in patient failed at least on two DMARD's.