Graft-versus-host disease

Source: Wikipedia, the free encyclopedia.
(Redirected from
Graft versus host disease
)
Not to be confused with
Host-versus-graft disease.
Graft-versus-host disease
Mouse colon impacted by acute graft-versus-host disease
SpecialtyEmergency medicine Edit this on Wikidata

Graft-versus-host disease (GvHD) is a

bone marrow transplants and stem cell transplants
.

White blood cells of the donor's immune system which remain within the donated tissue (the graft) recognize the recipient (the host) as foreign (non-self). The white blood cells present within the transplanted tissue then attack the recipient's body's cells, which leads to GvHD. This should not be confused with a transplant rejection, which occurs when the immune system of the transplant recipient rejects the transplanted tissue; GvHD occurs when the donor's immune system's white blood cells reject the recipient. The underlying principle (alloimmunity) is the same, but the details and course may differ.

GvHD can also occur after a blood transfusion, known as Transfusion-associated graft-versus-host disease or TA-GvHD if the blood products used have not been gamma irradiated or treated with an approved leukocyte reduction system. In contrast to organ/tissue transplant associated GvHD, the incidence of TA-GvHD is increased with HLA matching (first-degree or close relatives).[1]

Types

Micrographs of grades of skin graft-versus-host disease: Ranging from grade I GvHR (with minimal vacuolization in the epidermis) to grade II GvHR (with vacuolization and dyskeratotic bodies) to grade III GvHR (with sub epidermal cleft formation) and finally to grade IV GvHR (with separation of the dermis from the epidermis)[2]

In the clinical setting, graft-versus-host disease is divided into

chronic forms, and scored or graded on the basis of the tissue affected and the severity of the reaction.[3][4]

In the classical sense, acute graft-versus-host disease is characterized by selective damage to the

exocrine glands.[7]

Mucosal damage to the

scarring, and appears in both acute and chronic GvHD. This can result in an inability to have sexual intercourse.[8]

Acute

The acute or fulminant form of the disease (aGvHD) is normally observed within the first 10 to 100 days post-transplant,

human leukocyte antigens (HLA) matches between donor and the patient.[10]

The first signs are usually a rash, burning, and redness of the skin on the palms and soles. This can spread over the entire body. Other symptoms can include nausea, vomiting, stomach cramps, diarrhea (watery and sometimes bloody), loss of appetite, jaundice, abdominal pain, and weight loss.[10]

Acute GvHD of the

GI tract can result in severe intestinal inflammation, sloughing of the mucosal membrane, severe diarrhea, abdominal pain, nausea, and vomiting.[12] This is typically diagnosed via intestinal biopsy. Liver GvHD is measured by the bilirubin level in acute patients.[13] Skin GvHD results in a diffuse red maculopapular rash,[14]
sometimes in a lacy pattern.

Acute GvHD is staged as follows: overall grade (skin-liver-gut) with each organ staged individually from a low of 1 to a high of 4. Patients with grade IV GvHD usually have a poor prognosis. If the GvHD is severe and requires intense immunosuppression involving steroids and additional agents to get under control, the patient may develop severe infections[12] as a result of the immunosuppression and may die of infection. However, a 2016 study found that the prognosis for patients with grade IV GvHD has improved in recent years.[15]

Chronic

The chronic form of graft-versus-host disease (cGvHD) normally begins 90 to 600 days post-transplant.[10] The appearance of moderate to severe cases of cGVHD adversely influences long-term survival.[16]

The first symptom of cGvHD is commonly a rash on the palms of the hands or the soles of the feet, and the rash can spread and is usually itchy and dry. In severe cases, the skin may blister and peel, like a bad sunburn. A fever may also develop. Other symptoms of chronic GVHD can include:[10]

  • Decreased appetite
  • Diarrhea
  • Abdominal (belly) cramps
  • Weight loss
  • Yellowing of the skin and eyes (jaundice)
  • Enlarged liver
  • Bloated abdomen (belly)
  • Pain in the upper right part of the abdomen (belly)
  • Increased levels of liver enzymes in the blood (seen on blood tests)
  • Skin that feels tight
  • Dry, burning eyes
  • Dryness or painful sores in the mouth
  • Burning sensations when eating acidic foods
  • Bacterial infections
  • Blockages in the smaller airways of the lungs

In the

squamous cell carcinoma[17] in comparison to the classical oral lichen planus. Oral cancer associated with graft-versus-host disease may have more aggressive behavior with poorer prognosis, when compared to oral cancer in non-hematopoietic stem cell transplantation patients.[15]

Causes

GvHD pathology

Three criteria, known as the Billingham criteria, must be met in order for GvHD to occur.[18]

  • An
    immuno-competent
    graft is administered, with viable and functional immune cells.
  • The recipient is immunologically different from the donor –
    histo-incompatible
    .
  • The recipient is
    immunocompromised and therefore cannot destroy or inactivate the transplanted cells. In particular, it involves an inability of the recipient's cell-mediated immunity to destroy or inactivate viable lymphocytes from the donor.[19]

After bone marrow transplantation,

minor histocompatibility antigens) that can be presented by major histocompatibility complex (MHC) molecules to the donor's T-cells, which see these antigens as foreign and so mount an immune response.[22]

Antigens most responsible for graft loss are HLA-DR (first six months), HLA-B (first two years), and HLA-A (long-term survival).[23]

While donor T-cells are undesirable as effector cells of graft-versus-host disease, they are valuable for engraftment by preventing the recipient's residual

graft-versus-tumor effect.[25]

Transfusion-associated GvHD

Main article:
Transfusion-associated graft versus host disease

This type of GvHD is associated with

heterozygous for an HLA haplotype. It is associated with higher mortality (80–90%) due to involvement of bone marrow lymphoid tissue, however the clinical manifestations are similar to GVHD resulting from bone marrow transplantation. Transfusion-associated GvHD is rare in modern medicine. It is almost entirely preventable by controlled irradiation of blood products to inactivate the white blood cells (including lymphocytes) within.[26]

Thymus transplantation

negative selection to recognize self-antigens, and could therefore still mistake own structures in the rest of the body for being non-self. This is a rather indirect GvHD because it is not directly cells in the graft itself that causes it but cells in the graft that make the recipient's T cells act like donor T cells. It can be seen as a multiple-organ autoimmunity in xenotransplantation experiments of the thymus between different species.[27] Autoimmune disease is a frequent complication after human allogeneic thymus transplantation, found in 42% of subjects over one year post-transplantation.[28] However, this is partially explained by the fact that the indication itself, that is, complete DiGeorge syndrome, increases the risk of autoimmune disease.[29]

Thymoma-associated multiorgan autoimmunity (TAMA)

A GvHD-like disease called thymoma-associated multiorgan autoimmunity (TAMA) can occur in patients with thymoma. In these patients rather than a donor being a source of pathogenic T cells, the patient's own malignant thymus produces self-directed T cells. This is because the malignant thymus is incapable of appropriately educating developing thymocytes to eliminate self-reactive T cells. The result is a disease virtually indistinguishable from GvHD.[30]

Mechanism

The pathophysiology of GvHD includes three phases:[31]

  1. The afferent phase: activation of APC (
    antigen presenting cells
    )
  2. The efferent phase: activation, proliferation, differentiation and migration of effector cells
  3. The effector phase: target tissue destruction

Activation of APC occurs in the first stage of GvHD. Prior to haematopoietic stem cell transplantation, radiation or chemotherapy results in damage and activation of host tissues, especially intestinal mucosa. This allows the microbial products to enter and stimulate pro-inflammatory cytokines such as

TNF-α. These proinflammatory cytokines increase the expression of MHC and adhesion molecules on APCs, thereby increasing the ability of APC to present antigen.[32]
The second phase is characterized by the activation of effector cells. Activation of donor T-cells further enhances the expression of MHC and adhesion molecules, chemokines and the expansion of CD8 + and CD4 + T-cells and guest B-cells. In the final phase, these effector cells migrate to target organs and mediate tissue damage, resulting in multiorgan failure.[33]

Prevention

Treatment

Glucocorticoids

Intravenously administered

glucocorticoids, such as prednisone, are the standard of care in acute GvHD[11] and chronic GVHD.[41] The use of these glucocorticoids is designed to suppress the T-cell-mediated immune onslaught on the host tissues; however, in high doses, this immune-suppression raises the risk of infections and cancer relapse. Therefore, it is desirable to taper off the post-transplant high-level steroid doses to lower levels, at which point the appearance of mild GVHD may be welcome, especially in HLA mis-matched patients, as it is typically associated with a graft-versus-tumor effect.[citation needed].While glucocorticoids remain the first line of treatment for acute GVHD, only about 50% of patients respond to treatment, otherwise having steroid-refractory GVHD (SR-GVHD).[42] An increasing number of recent treatment options for SR-GVHD have been investigated, such as extracorporeal photopheresis (ECP), mesenchymal stem cell (MSCs), fecal microbial transplantation (FMT), and the medication Ruxolitinib.[42]

Steroid-sparing immunosuppression/immunomodulation

calcineurin inhibitors. The substances are structurally different but have the same mechanism of action. Cyclosporine binds to the cytosolic protein peptidyl-prolyl cis-trans isomerase A (known as cyclophilin), while tacrolimus binds to the cytosolic protein peptidyl-prolyl cis-trans isomerase FKBP12. These complexes inhibit calcineurin, block dephosphorylation of the transcription factor NFAT of activated T-cells and its translocation into the nucleus.[43] Standard prophylaxis involves the use of cyclosporine for six months with methotrexate. Cyclosporin levels should be maintained above 200 ng/ml.[44]

Other substances that have been studied for GvHD treatment include, for example: sirolimus, pentostatin, etanercept, and alemtuzumab.[44]

In August 2017, the

US FDA approved ibrutinib to treat chronic GvHD after failure of one or more other systemic treatments.[45]

Clinical research

There are a large number of clinical trials either ongoing or recently completed in the investigation of graft-versus-host disease treatment and prevention.[46]

On May 17, 2012, Osiris Therapeutics announced that Canadian health regulators approved

stem cell drug to be approved for a systemic disease.[47]

In January 2016, Mesoblast released results of a phase 2 clinical trial on 241 children with acute Graft-versus-host disease, that was not responsive to steroids.[48] The trial was of a mesenchymal stem cell therapy known as remestemcel-L or MSC-100-IV. Survival rate was 82% (vs 39% of controls) for those who showed some improvement after one month, and in the long term 72% (vs 18% of controls) for those that showed little effect after one month.[48]

HIV elimination

Graft-versus-host disease has been implicated in eliminating several cases of HIV, including

The Berlin Patient and six others in Spain.[49]

See also

References

  1. PMID 9875072
    .
  2. PMID 28373870
    .
  3. S2CID 24811357
    .
  4. PMID 16338616
    .
  5. PMID 26209034
    .
  6. PMID 20371463
    .
  7. S2CID 39209313
    .
  8. PMID 14677115
    .
  9. PMID 27982319
    .
  10. ^ a b c d e f "Stem Cell or Bone Marrow Transplant Side Effects". www.cancer.org. Retrieved 2020-09-01.
  11. ^
    PMID 11274753
    .
  12. ^ a b "Graft-versus-host disease". MedlinePlus. National Library of Medicine. Retrieved 6 May 2019.
  13. PMID 22296496
    .
  14. S2CID 25151282
    .
  15. ^
    PMID 26748160
    .
  16. PMID 12720215
    .
  17. PMID 30726819
    .
  18. PMID 4875305
    .
  19. PMID 7927137.{{cite journal}}: CS1 maint: multiple names: authors list (link
    )
  20. S2CID 1585777
    .
  21. S2CID 73449161
    .
  22. PMID 21727137
    .
  23. PMID 25516409
    .
  24. PMID 29222323
    .
  25. PMID 18539902
    .
  26. S2CID 7462268
    .
  27. S2CID 24007739
    .
  28. S2CID 219575147
    .
  29. PMID 17284531
    .
  30. PMID 17433850
    .
  31. PMID 28373413
    .
  32. S2CID 7043844
    .
  33. S2CID 25250676
    .
  34. S2CID 6859250
    .
  35. S2CID 6486524
    .
  36. PMID 11407342
    .
  37. PMID 27662016
    .
  38. PMID 30697701
    .
  39. PMID 8054913
    .
  40. S2CID 33732870
    .
  41. S2CID 27292769
    .
  42. ^
    PMID 36923700
    .
  43. S2CID 22094672
    .
  44. ^ a b Mandanas RA. "Graft Versus Host Disease Treatment & Management: Medical Care". Medscape. Retrieved 30 August 2017.
  45. ^ Research, Center for Drug Evaluation and (February 9, 2019). "FDA expands ibrutinib indications to chronic GVHD". FDA – via www.fda.gov.
  46. ^ "Search of: Graft-versus-host disease - List Results - ClinicalTrials.gov". clinicaltrials.gov.
  47. ^ "World's First Stem-Cell Drug Approval Achieved in Canada". The National Law Review. Drinker Biddle & Reath LLP. 2012-06-12. Retrieved 2012-07-01.
  48. ^ a b "Increased Survival Using MSB Cells In Children With aGVHD". Retrieved 22 Feb 2016.
  49. ^ "Immune war with donor cells after transplant may wipe out HIV". ?. NewScientist. 2017-05-03. Retrieved 2018-11-23.

Further reading

External links

Retrieved from "https://en.wikipedia.org/w/index.php?title=Graft-versus-host_disease&oldid=1196948513"