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Preventing GvHD

Find out how your doctor will reduce your risk of developing GvHD.

Getting the best donor match

GvHD can develop when the donor and the person receiving donor cells have a different tissue type. So your transplant specialist will make sure your donor is as closely matched to you as possible. This is called tissue typing and helps reduce your risk of GvHD.

Tissue typing

The HLA (human leukocyte antigen) system describes the proteins found on your blood cells. Your doctors aim to find a donor with the closest HLA match possible.

Doctors usually test for 5 pairs of major HLA antigens. This gives a total of 10 antigens. We inherit one half of the pair from each of our parents. When choosing a donor, doctors aim to match 10 out of 10 HLA proteins. But it may be possible to do a transplant if they don't all match.

Finding a donor

We inherit the proteins from our parents so your best chance of a match is with a relative. You have a 1 in 4 (25%) chance of an exact match if you have a brother or sister. Other members of family can be tested if you don’t have siblings or if they don’t match your tissue type. Parents may be a close enough match.

Your doctor will search for a bone marrow match on a register of the general population if no one in your family is a match. Registers are kept by the British Bone Marrow Registry (NHSBT) and the Anthony Nolan Trust. Another possibility is to look at cord blood registries. These contain blood taken from umbilical cords at births, which can be used as a source of stem cells.

About T cells

Before and after your transplant, your doctors will use treatments to reduce the chance of GvHD. These treatments destroy T cells.

T cells are white blood cells that are part of the immune system. They attack cells that are foreign to the body. GvHD happens when T cells in the donated bone marrow or stem cells (the graft) attack your own body cells (the host).

So reducing the number of T cells in the donor marrow or stem cells (the graft) reduces GvHD.

Sometimes GvHD is a good thing. The T cells in the graft will also attack any remaining cancer cells. This reduces the risk of your disease coming back. This is called the graft versus disease effect. Doctors try to strike a balance between preventing severe GvHD and getting some possible benefits from mild GvHD.

To lower your risk of GvHD you might have treatment:

  • before your transplant
  • to remove T cells from the bone marrow or stem cells
  • after your transplant

Treatment before your transplant

Before your transplant you have a drug to reduce the number of T cells in your donated marrow or stem cells. You usually have a drug called ciclosporin which is also called Deximune, Neoral or Sandimmum.

You start having it by drip (intravenously) a couple of days before your transplant. Before you go home you start taking it daily as a capsule.

You should never take it with grapefruit or grapefruit juice because this can change the way the drug works

You usually keep taking ciclosporin for about 6 months after the transplant. As an alternative to ciclosporin, you might take a combination of mycophenolate mofetil (MMF) and tacrolimus.

You might have treatment with other drugs before your transplant, such as:

  • alemtuzumab (Campath)
  • antithymocytic globulin (ATG)
  • newer drugs, including sirolimus (Rapamide)

Removing T cells from the bone marrow or stem cells

Your doctors can remove T cells from your donor’s bone marrow after it has been donated, or during the donation of stem cells. This is called T cell depletion. It isn't commonly used.

Treatment after transplant

You have treatment with drugs after your transplant to reduce the risk of GvHD.

Methotrexate

Low doses of the chemotherapy drug methotrexate suppresses your immune system. This helps to keep the T cells down and so stops them attacking your body cells.

Cyclophosphamide

You may have a chemotherapy drug called cyclophosphamide after a stem cell transplant. This is more likely after a half matched transplant from a family member, usually a parent or child. This is called a haploidentical transplant. The donor is a 50% match with the person having the transplant.

Before the transplant, you have chemotherapy to lower your immune system. These are usually lower doses of chemotherapy than in a traditional stem cell transplant. This is called reduced intensity conditioning.

A few days after the transplant, you have a high dose of cyclophosphamide. The donor's immune cells recognise your body cells as foreign, and start to multiply to attack them. The cyclophosphamide kills these rapidly growing immune cells, and so stops them attacking your body cells. This reduces side effects such as GvHD. You may have this treatment as part of a clinical trial.

Last reviewed: 
10 Nov 2017
  • Graft-versus-host disease
    BMJ Best Practice website (Accessed November 2017)

  • Prophylaxis and treatment of GVHD: EBMT–ELN working group recommendations for a standardized practice
    T Ruutu and others
    Bone Marrow Transplantation, 2014. Volume 49, Pages 168-173

  • Essential Haematology (7th edition)
    V Hoffbrand
    Wiley-Blackwell, 2015

  • DeVita, Hellman, and Rosenberg's Cancer: Principles & Practice of Oncology
    VT DeVita Jr, TS Lawrence and SA Rosenberg
    Lippincott Williams & Wilkins, 2015

  • Post-transplantation cyclophosphamide for tolerance induction in HLA-haploidentical bone marrow transplantation
    L Luznik and others
    Seminars of Oncology, 2012, Volume 39, Issue 6, Pages 683-93

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