AIRLINK 74.00 Decreased By ▼ -0.25 (-0.34%)
BOP 5.14 Increased By ▲ 0.09 (1.78%)
CNERGY 4.55 Increased By ▲ 0.13 (2.94%)
DFML 37.15 Increased By ▲ 1.31 (3.66%)
DGKC 89.90 Increased By ▲ 1.90 (2.16%)
FCCL 22.40 Increased By ▲ 0.20 (0.9%)
FFBL 33.03 Increased By ▲ 0.31 (0.95%)
FFL 9.75 Decreased By ▼ -0.04 (-0.41%)
GGL 10.75 Decreased By ▼ -0.05 (-0.46%)
HBL 115.50 Decreased By ▼ -0.40 (-0.35%)
HUBC 137.10 Increased By ▲ 1.26 (0.93%)
HUMNL 9.95 Increased By ▲ 0.11 (1.12%)
KEL 4.60 Decreased By ▼ -0.01 (-0.22%)
KOSM 4.83 Increased By ▲ 0.17 (3.65%)
MLCF 39.75 Decreased By ▼ -0.13 (-0.33%)
OGDC 138.20 Increased By ▲ 0.30 (0.22%)
PAEL 27.00 Increased By ▲ 0.57 (2.16%)
PIAA 24.24 Decreased By ▼ -2.04 (-7.76%)
PIBTL 6.74 Decreased By ▼ -0.02 (-0.3%)
PPL 123.62 Increased By ▲ 0.72 (0.59%)
PRL 27.40 Increased By ▲ 0.71 (2.66%)
PTC 13.90 Decreased By ▼ -0.10 (-0.71%)
SEARL 61.75 Increased By ▲ 3.05 (5.2%)
SNGP 70.15 Decreased By ▼ -0.25 (-0.36%)
SSGC 10.52 Increased By ▲ 0.16 (1.54%)
TELE 8.57 Increased By ▲ 0.01 (0.12%)
TPLP 11.10 Decreased By ▼ -0.28 (-2.46%)
TRG 64.02 Decreased By ▼ -0.21 (-0.33%)
UNITY 26.76 Increased By ▲ 0.71 (2.73%)
WTL 1.38 No Change ▼ 0.00 (0%)
BR100 7,874 Increased By 36.2 (0.46%)
BR30 25,599 Increased By 139.8 (0.55%)
KSE100 75,342 Increased By 411.7 (0.55%)
KSE30 24,214 Increased By 68.6 (0.28%)
Editorials

Scientists close to HIV cure in humans after treating mice through gene-editing

In light of a recent breakthrough where scientists cured HIV via gene-editing in living animals, scientists now bel
Published July 4, 2019 Updated July 8, 2019

In light of a recent breakthrough where scientists cured HIV via gene-editing in living animals, scientists now believe that they are closer to finding a cure for HIV for humans too.

For the first time ever, researchers have cured HIV, the virus that leads to AIDS, from the genes of living mice through CRISPR gene-editing. This discovery marks as a great achievement along the path to freeing humans from the lethal disease.

The team started by engineering mice to create human T cells susceptible to HIV infection. After infecting the mice, the researchers used a therapeutic strategy called long-acting slow-effective release antiretroviral therapy (LASER ART) in order to suppress HIV replication within mice, reported Futurism.

Gene-editing tech could make people immune to flu, HIV in future

In the end, the team then used CRISPR gene-editing technology for removing HIV DNA from the infected cells. After later analyzing the animals, it was discovered that about one-third of the animals showed no signs of HIV.

Next, the team plans on combining LASER ART and CRISPR therapy in non-human primates. If those trials go successful, the human trials will initiate within the year, as per researcher Kamel Khalili. However, though optimistic, they do realize the hurdles they would have to cross.

“Things that work in mice, may not work in men,” researcher Howard Gendelman told CNBC. “The limitations of any mouse work have to do with the species, how the drug is administered, the distribution, which is a lot easier than a man or a woman.”

Copyright Business Recorder, 2019

Comments

Comments are closed.