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Personalized medicine against hereditary immunodeficiency

Date:
August 14, 2014
Source:
Karolinska Institutet
Summary:
Researchers have found a method to repair the gene mutation causing agammaglobulinemia, an immunodeficiency disease that almost exclusively affects boys and in which the body lacks the ability to produce immunoglobulins (gamma globulin). The disease is characterized by recurring bacterial infections, mainly in the respiratory system, and persons who suffer from the illness currently need life-long gamma globulin treatment.

Researchers at Karolinska Institutet in Sweden have found a method to repair the gene mutation causing agammaglobulinemia, an immunodeficiency disease that almost exclusively affects boys and in which the body lacks the ability to produce immunoglobulins (gamma globulin). The disease is characterised by recurring bacterial infections, mainly in the respiratory system, and persons who suffer from the illness currently need life-long gamma globulin treatment.

"Although there is a lot of research left to be done, the findings indicate that we may be able to treat some patients in the future," says Edvard Smith, Professor at the Department of Laboratory Medicine at Karolinska Institutet and one of the researchers behind the study that is presented in the Journal of Clinical Investigation.

Agammaglobulinemia is a rare, hereditary disease that is caused by a mutation, which results in a lack of the enzyme BTK. BTK plays an important role in the signalling of white blood cells and thus in developing and maintaining an effective immune system. In the new study, the researchers show that it is possible to repair faulty RNA and recreate BTK in lymphocytes, white blood cells. The new study emanates from the same research group at Karolinska Institutet that previously identified the genetic basis for X-linked agammaglobulinemia (XLA).

It is previously known that synthetic building blocks for our genetic make-up (known as oligonucleotides) can modify the RNA and recreate truncated forms of the protein that is missing in severe muscular dystrophy. The new study shows that it is possible to experimentally correct the defect and recreate an intact BTK enzyme for a Swedish family with XLA. The therapy has been customised for this particular mutation and is thereby a genuine example of "personalised medicine." The researchers utilised molecular biological methods and created a mouse, which carries the gene in question. The mice also lacked enzymes of their own, as their corresponding gene was inactivated.

"We have been able to show how synthetic oligonucleotides can correct RNA both in patient cells in a test tube, and in living animals," says Edvard Smith.

The number of new cases of agammaglobulinemia is estimated at 6 in one million births, which means that there is roughly one boy born with the disease in Sweden every other year. BTK has received renewed attention as it has been discovered that the protein also plays an important role in various types of blood cancer that have their origin in immune cells. A new medicine that blocks the function of the BTK enzyme was recently approved for the treatment of leukaemia and lymphoma in the USA.

The study has been financed using funds from the Swedish Cancer Society, the Swedish Research Council and Stockholm County Council (ALF), among others.


Story Source:

The above story is based on materials provided by Karolinska Institutet. Note: Materials may be edited for content and length.


Journal Reference:

  1. Burcu Bestas, Pedro M.D. Moreno, K. Emelie M. Blomberg, Dara K. Mohammad, Amer F. Saleh, Tolga Sutlu, Joel Z. Nordin, Peter Guterstam, Manuela O. Gustafsson, Shabnam Kharazi, Barbara Piątosa, Thomas C. Roberts, Mark A. Behlke, Matthew J.A. Wood, Michael J. Gait, Karin E. Lundin, Samir EL Andaloussi, Robert Mεnsson, Anna Berglφf, Jesper Wengel, C.I. Edvard Smith. Splice-correcting oligonucleotides restore BTK function in X-linked agammaglobulinemia model. Journal of Clinical Investigation, 2014; DOI: 10.1172/JCI76175

Cite This Page:

Karolinska Institutet. "Personalized medicine against hereditary immunodeficiency." ScienceDaily. ScienceDaily, 14 August 2014. <www.sciencedaily.com/releases/2014/08/140814123840.htm>.
Karolinska Institutet. (2014, August 14). Personalized medicine against hereditary immunodeficiency. ScienceDaily. Retrieved September 17, 2014 from www.sciencedaily.com/releases/2014/08/140814123840.htm
Karolinska Institutet. "Personalized medicine against hereditary immunodeficiency." ScienceDaily. www.sciencedaily.com/releases/2014/08/140814123840.htm (accessed September 17, 2014).

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