Для защиты от ВИЧ отредактированы Т-клетки человека
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29.07.2015
Используя популярную систему редактирования генома, американские ученые из Калифорнийского университета впервые разработали новую стратегию, чтобы точно изменять Т-клетки человека, также называемые иммунными клетками.
Эти клетки иммунной системы играют важную роль в широком спектре заболеваний от диабета до СПИДа и рака поэтому достижение ученых дает универсальный новый инструмент для исследования функций Т-клеток. Данное открытие также дает новые возможности для лечения, основанного на системе редактирования генома, известного как CRISPR/Cas9, для многих серьезных проблем со здоровьем.
При помощи нового подхода специалисты смогли отключить белок под названием CXCR4 на поверхности Т-клеток, который может быть использован ВИЧ при заражении клеток. Исследователям также удалось отключить белок PD-1, который вызвал большой интерес в области иммунотерапии рака. Использование препаратов, блокирующих PD-1, заставляет Т-клетки атаковать опухоли.
Система редактирования генома захватила воображение как ученых, потому что оно позволяет легко и недорого редактировать генетическую информацию практически в любом организме. Т-клетки, которые циркулируют в крови, являются очевидным кандидатом медицинского применения данной технологии. Эти клетки могут быть легко собраны из пациентов, отредактированы при помощи системы CRISPR/Cas9, а затем возвращены обратно в организм, чтобы оказывать терапевтический эффект.
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Сотрудникам Калифорнийского университета в Сан-Франциско удалось успешно изменить Т-клетки иммунной системы человека. Для этого ученые использовали систему CRISPR/Cas9, позволяющую редактировать геном.
На первом этапе авторы исследования убрали с поверхности клеток белок CXCR4, который используется для проникновения вируса иммунодефицита человека (ВИЧ) внутрь клетки. Кроме того, ученые «выключили» белок PD-1. Ранее проведенные исследования показали, что препараты, блокирующие этот белок, способствуют активации Т-клеток, которые начинают атаковать опухолевые клетки.
Как пояснили ученые, чье исследование будут опубликовано в журнале Proceedings of the National Academy of Sciences, они изменили технологию и упростили метод доставки нуклеазы Cas9 и gRNA молекул РНК, которые контролируют процесс вставки или удаления уридиновых нуклеотидов в мРНК. Для этого авторы исследования использовали метод электропорации, обеспечивающий повышение проницаемости клеточных мембран. Таким образом рибонуклеотиды Cas9, то есть gRNA в комплексе с этим ферментом, эффективнее доставлялись внутрь клетки.
Несмотря на то, что система CRISPR/Cas9 активно используется в исследованиях, ученые пояснили, что в случае с Т-клетками редактирование генома оказалось очень непростой задачей. «Наш случай был своеобразным вызовом для этой сферы науки. Мы потратили полтора года на то, чтобы оптимизировать процесс редактирования генома Т-клеток. Существует много возможных вариантов терапевтического применения нашей разработки», объяснил соавтор исследования Александр Марсон (Alexander Marson).
Источник: Ученые отредактировали Т-клетки человека для защиты от ВИЧ | http://medportal.ru/mednovosti/news/2015/07/28/548cells/ |
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Source: University of California - San Francisco | In CRISPR advance, scientists successfully edit human T cells | Research has implications for autoimmune diseases, AIDS, cancer | http://www.sciencedaily.com/releases/2015/07/150727153727.htm |
Summary: Scientists have devised a new strategy to precisely modify human T cells using the genome-editing system known as CRISPR/Cas9. Because these immune-system cells play important roles in a wide range of diseases, from diabetes to AIDS to cancer, the achievement provides a versatile new tool for research on T cell function, as well as a path toward CRISPR/Cas9-based therapies for many serious health problems.
In a project spearheaded by investigators at UC San Francisco, scientists have devised a new strategy to precisely modify human T cells using the genome-editing system known as CRISPR/Cas9. Because these immune-system cells play important roles in a wide range of diseases, from diabetes to AIDS to cancer, the achievement provides a versatile new tool for research on T cell function, as well as a path toward CRISPR/Cas9-based therapies for many serious health problems.
Using their novel approach, the scientists were able to disable a protein on the T-cell surface called CXCR4, which can be exploited by HIV when the virus infects T cells and causes AIDS. The group also successfully shut down PD-1, a protein that has attracted intense interest in the burgeoning field of cancer immunotherapy, as scientists have shown that using drugs to block PD-1 coaxes T cells to attack tumors.
The CRISPR/Cas9 system has captured the imagination of both scientists and the general public, because it makes it possible to easily and inexpensively edit genetic information in virtually any organism. T cells, which circulate in the blood, are an obvious candidate for medical applications of the technology, as these cells not only stand at the center of many disease processes, but could be easily gathered from patients, edited with CRISPR/Cas9, then returned to the body to exert therapeutic effects.
But in practice, editing T cell genomes with CRISPR/Cas9 has proved surprisingly difficult, said Alexander Marson, PhD, a UCSF Sandler Fellow, and senior and co-corresponding author of the new study. "Genome editing in human T cells has been a notable challenge for the field," Marson said. "So we spent the past year and a half trying to optimize editing in functional T cells. There are a lot of potential therapeutic applications, and we want to make sure we're driving this as hard as we can."
The new work was done under the auspices of the Innovative Genomics Initiative (IGI), a joint UC Berkeley-UCSF program co-directed by Berkeley's Jennifer Doudna, PhD, and Jonathan Weissman, PhD, professor of cellular and molecular pharmacology at UCSF and a Howard Hughes Medical Institute (HHMI) investigator. Marson is an affiliate member of the IGI.
Doudna, professor of chemistry and of cell and molecular biology at Berkeley, and an HHMI investigator, said that the research is a significant step forward in bringing the power of CRISPR/Cas9 editing to human biology and medicine. "It's been great to be part of this exciting collaboration, and I look forward to seeing the insights from this work used to help patients in the future," said Doudna, co-corresponding author of the new paper.
Cas9, an enzyme in the CRISPR system that makes cuts in DNA and allows new genetic sequences to be inserted, has generally been introduced into cells using viruses or circular bits of DNA called plasmids. Then, in a separate step, a genetic construct known as single-guide RNA, which steers Cas9 to the specific spots in DNA where cuts are desired, is also placed into the cells.
Until recently, however, editing human T cells with CRISPR/Cas9 has been inefficient, with only a relatively small percentage of cells being successfully modified. And while scientists have had some success in switching off genes by inserting or deleting random sequences, they have not yet been able to use CRISPR/Cas9 to paste in (or "knock in") specific new sequences to correct mutations in T cells.
As will be reported online in Proceedings of the National Academy of Sciences during the week of July 27, 2015, a team led by first authors Kathrin Schumann, PhD, a postdoctoral fellow in Marson's laboratory, and Steven Lin, PhD, a postdoctoral fellow in the Doudna lab, cracked these problems by streamlining the delivery of Cas9 and single-guide RNA to cells.
In lab dishes, the group assembled Cas9 ribonucleoproteins, or RNPs, which combine the Cas9 protein with single-guide RNA. They then used a method known as electroporation, in which cells are briefly exposed to an electrical field that makes their membranes more permeable, to quickly deliver these RNPs to the interior of the cells.
With these innovations, the researchers successfully edited CXCR4 and PD-1, even knocking in new sequences to replace specific genetic "letters" in these proteins. The group was then able to sort the cells using markers expressed on the cell surface, to help pull out successfully edited cells for research, and eventually for therapeutic use.
"We tried for a long time to introduce Cas9 with plasmids or lentiviruses, and then to express separately the single-guide RNA in the cell," Schumann said. "Using RNPs made outside the cell, so that the cell is responsible for as little of the process as possible, has made a big difference."
Marson stressed that, while recent reports of CRISPR/Cas9 editing of human embryos have stirred up controversy, T cells are created anew in each individual, so modifications would not be passed on to future generations. He hopes that Cas9-based therapies for T cell-related disorders, which include autoimmune diseases as well as immunodeficiencies such as "bubble boy disease," will enter the clinic in the future.
"There's actually well-trodden ground putting modified T cells into patients. There are companies out there already doing it and figuring out the safety profile, so there's increasing clinical infrastructure that we could potentially piggyback on as we work out more details of genome editing," Marson said. "I think CRISPR-edited T cells will eventually go into patients, and it would be wrong not to think about the steps we need to take to get there safely and effectively."
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