Advertisement

Donor Selection

  • Mairéad Níchonghaile
Open Access
Chapter

Abstract

Allogeneic haematopoietic stem cell transplant (HSCT) is the treatment of choice for a variety of malignant and non-malignant disorders. The aim of HSCT is to replace the patient’s haematopoiesis with that taken from a donor, and a prerequisite is the identification of a suitable donor. It is an intense and demanding process and puts considerable strain on both recipients and donors. The choice of donor has an impact on the transplantation process from scheduling to outcome. There are several common donor issues whether the donor is related or unrelated including eligibility, confidentiality, informed consent and right to refuse consent.

Keywords

Eligibility Confidentiality Informed consent Donation HLA match Donor selection 

3.1 Introduction

Allogeneic haematopoietic stem cell transplant (HSCT) is the treatment of choice for a variety of malignant and non-malignant conditions. The aim of HSCT is to replace the patient’s haematopoiesis with that taken from a donor, and a prerequisite is the identification of a suitable donor. There are three conditions which have to be met for a donor to be considered suitable – the donor needs to be suitably matched, healthy and willing to donate (Kisch 2015). Allogeneic HSCT is an intense and demanding process and puts considerable strain on both recipients and donors.

Donors can be related or unrelated (Fig. 3.1), and the primary consideration is the degree of HLA compatibility of the donor to the recipient and this is considered the most important factor to determining overall success and the transplant-related mortality (Kulkarm and Treleaven 2009).
Fig. 3.1

Types of donors

3.2 Human Leukocyte Antigens

Human leukocyte antigens (HLA) are part of the major histocompatibility complex and is highly polymorphic, meaning that there are a lot of variations of the HLA type with humans, and they are found on the short arm of chromosome 6. The primary role of HLA molecules is to preserve peptide to T cells, enabling them to recognise and eliminate “foreign” particles present in an individual and also to prevent the recognition of self as foreign. Due to the Mendelian1 inheritance of HLA types, the first place to look for a potential donor is within the immediate family (Fig. 3.2). Our HLA type is inherited from our parents – one haplotype from each parent giving rise to a one in four chance that sibling may match another.
Fig. 3.2

HLA typing

Table 3.1 shows the wide variety and number of HLA alleles (the variant forms of the gene) that have been identified. HLA typing can be serological or DNA based though currently the majority of HLA typing is DNA based.
Table 3.1

The number of HLA alleles currently named at each locus (April 2011)

HLA locus

Number of class I alleles

HLA locus

Number of class II alleles

HLA–A

1601

HLA–DRB

1027

HLA–B

2125

HLA–DQA1

44

HLA–C

1102

HLA–DQB1

153

  

HLA–DPA1

32

  

HLA–DPB1

149

EBMT Handbook 6th Edition (2012) page 76

Table 3.2 shows an example of the nomenclature used for HLA typing. HLA typing looks at matching recipients and donors at HLAs A, B and C (class I typing) and HLAs DR, DQ and DP (class II typing). The nomenclature used is the gene name followed by an asterisk with a four-digit allele name; the first two digits indicated the serological groups and the last two digits the number of the allele within the group.
Table 3.2

An example of HLA nomenclature and its relation to HLA typing techniques

Typing method

Nomenclature

Serological

A1

DNA based: Low resolution

A*01

DNA based: Low resolution

A*01:01/01:4 N

DNA based: Low resolution

A*01:01

EBMT Handbook 6th Edition (2012) page 77

When we speak of matching, we describe the potential donors as being fully matched (6/6 within the related setting or 10/10 when referring to unrelated donor), a one- or two-antigen mismatch or a haplotype match (i.e. 3/6 or 5/10). The example below shows a patent and his potential sibling donors.

Below is a list of examples when describing degrees of HLA matching between recipient and potential donor.

The possibility of having a suitably matched sibling donor varies depending on ethnicity as distinct HLA types that occur differ among ethnic groups and family size. If a suitable matched sibling donor is not available, a search can be undertaken of the volunteer unrelated donor panels that are part of BM Donors Worldwide. There are now in excess of 18 million volunteer unrelated donors registered on these panels.

Gragert et al. (2014) published the chances of identifying a suitable matched donor for a recipient requiring allogeneic HSCT. While a person of Caucasian background has a relatively good chance of identifying a potential donor, some ethnic groups have a much lower probability of finding a match through unrelated donor searching. This has led to an increase in the use of alternate donors, e.g. a haploidentical donors or alternative cell sources, e.g. cord blood stem cells. The use of haploidentical transplantation with improved conditioning and GVHD prophylaxis means that nearly all patients will gave the potential of a haploidentical donor (Table 3.3).
Table 3.3

Likelihood of identifying HLA-matched adult donors and cord blood units

U.S. Racial and Ethnic Group

Likelihood of identifying an adult donora

Likelihood of identifying a cord-blood unit for patients ≥20 Yr of ageb

Likelihood of identifying a cord-blood unit for patients <20 Yr of age?

8/8 HLA match

≥7.8 HLA match

6/6 HLA match

≥5/6 HLA match

≥4/6 HLA match

6/6 HLA match

≥5/6 HLA match

≥4/6 HLA match

   

Percent

    

White European

75

97

17

66

96

38

87

99

Middle Eastern or North African

46

90

6

46

91

18

75

98

African American

19

76

2

24

81

6

58

95

African

18

71

1

23

81

5

56

95

Black South or Central American

16

66

2

27

82

7

58

96

Black Caribbean

19

74

1

24

81

6

58

95

Chinese

41

88

6

44

91

19

77

98

Korean

40

87

5

39

89

17

73

98

South Asian

33

84

4

41

90

14

73

98

Japanese

37

87

4

37

88

16

72

97

Filipino

40

83

5

42

89

19

76

98

Southeast Asian

27

76

3

37

89

12

70

98

Vietnarnese

42

84

6

44

89

20

76

98

Hawaiian or Pacific Islander

27

72

3

32

84

10

64

96

Mexican

37

87

6

45

91

19

75

98

Hispanic South or Central American

34

80

5

43

90

17

73

98

Hispanic Caribbean

40

83

5

40

89

17

71

98

Native North American

52

91

10

54

93

25

80

99

Native South or Central American

49

87

11

53

93

26

79

98

Native Caribbean

32

77

4

35

86

14

66

97

Native Alaskan

36

83

7

47

91

18

75

98

Gragert et al. 2014

aData are the probabilities of identifying an adult donor who is available

bData are the probabilities of identifying a unit with an adequate cell dose

3.3 Eligibility for HLA Typing of Potential Related Donors

Every institution will have their own requirements regarding eligibility to be HLA typed, and there should be a policy available locally. The main eligibility criteria is willingness to be tested – this does not imply consent to donation – and that the potential donor is not suffering from any conditions that may be a threat or a risk to the recipient or that may be aggravated in themselves by the donation process. As a result potential donors who have had a malignancy previously or have an autoimmune condition should be excluded or given special consideration. Relevant guidance can be found at http://www.worldmarrow.org/donorsuitability/index.php/Main_Page#Related_donors

Sibling donors actively participate in the quest for a cure for their sibling, but this exposes them to an invasive medical procedure that can lead to stress and anxiety and places them in a complex situation. While it can have a beneficial effect for the donor and the family unit as a whole, donors often feel responsible for the recipient outcome.

With respect to unrelated donors, each registry will have their own inclusion/exclusion criteria, but they usually follow the advice of the WMDA (World Marrow Donor Association) on whose website there is comprehensive guidance with respect to donor eligibility. To be listed as a volunteer donor on a blood stem cell registry, you must be:
  • Between 18 and 60 years old (age limits may vary per country)

  • In good health

  • Ready to donate stem cells to any patient in need

To donate umbilical cord blood, a future mother must generally be:
  • Over 18 years of age

  • In good health

  • Pregnant without complications

  • Registered well before the onset of labour

3.4 Algorithm of Donor Choice and Selection

Many factors affect the choice of donor, and with the selection of donor sources now available, the possibility of offering HSCT has extended to almost all patients who require it (Apperley et al. 2012).

3.4.1 Donor Selection

The main determinants when selecting a donor whether related or unrelated are as follows:

The “perfect” donor does not exist – no current algorithm will guarantee a positive outcome will always occur.

3.4.2 HLA Match

The most significant factor in success and overall outcome is the degree of match between the donor and recipient.
  1. 1.

    Most data suggest a 10/10 match is the best choice.

     
  2. 2.

    In many circumstance a 9/10 match can be considered as good as a 10/10 but where the mismatch occurs is important. A mismatch at HLA DQB1 has been shown to have the least likely adverse outcome. Worse outcomes have been seen where the mismatch is at class I. Choosing a HLA A, B or C mismatch should be based on local studies and experience as it can be population or ethnically dependent.

     
  3. 3.

    Two or more mismatches are associated with a poorer outcome (Shaw 2009).

     

3.4.3 Cytomegalovirus (CMV) Status

Cytomegalovirus (CMV) is a common virus that can infect almost anyone. Most people don’t know they have CMV because it rarely causes symptoms. However, if you’re pregnant or have a weakened immune system, CMV is cause for concern. Once infected with CMV, your body retains the virus for life.

Where possible the donor-recipient pairing should be CMV matched with preference given to a CMV compatible donor, i.e. negative donor in a CMV-negative recipient. The CMV status of the donor is less important in a CMV-positive recipient, but there is some evidence that a CMV-positive donor is preferable in a CMV-positive recipient as it may protect the patient from CMV infection (Rovira et al. 2012). Analysis has shown that prior donor CMV exposure significantly reduces the risk of CMV reactivation in CMV-positive recipients as immunity against CMV seems to be transferred with the donor cells and protects CMV-positive recipients from reactivation.

3.4.4 Blood Group

Blood group mismatch is not a contraindication to HSCT, and there is conflicting data about the role of blood group mismatch in relation to post HSCT relapse, but the majority of research suggest that is does not influence HSCT outcome (Kulkarni and Treleaven 2009).

Matching donor and recipient blood group may benefit the recipient as it may reduce the number of transfusions and the period of transfusion dependency post HSCT. Blood group matching is an important consideration in transplants where BM stem cells are the product of choice as it removes the requirement for the product to be red cell depleted to reduce the risk of intravascular haemolysis in the recipient.

3.4.5 Sex Match

Donor-recipient sex match is an important predictor of transplant-related mortality (TRM) with the combination of a male recipient with a female donor known to have an increased risk of chronic GVHD and a higher TRM but not necessarily a reduced relapse risk in all diseases.

3.4.6 Parity

If only female donors are available, it is recommended where possible to use a nonparous female donor as -parous females have a higher chance of having HLA-specific antibodies due to exposure to foetal antigens in utero. It is accepted that recipients (either male or female) who have a HSCT from parous donors have a higher risk of chronic GVHD (Kollman et al. 2001).

3.4.7 Age

The younger the donor at the time of HSCT donation has a favourable outcome after HSCT. It appears that the risk of acute GVHD (Grade 3 or above) and chronic GVHD is higher, and overall survival can be lower with increased donor age (Kollman et al. 2001).

3.4.8 Donor Evaluation

All donors should be medically assessed and consented independently from the recipient medical team. The maxim of “Do No Harm” to the donor is paramount, and no donor should be selected where there is a risk of aggravating or exacerbating a potential medical issue in the donor.

Table 3.4 lists the investigations that should be undertaken for all donors. There is a concern that related donors may not always be as forthcoming about their health as they do not wish to jeopardise their relative’s transplant. The table lists the mandatory virology screening that is required on all donors – specific or additional testing may be required in certain countries, e.g. screening for West Nile virus if donor resides in an at risk area, or if the countries’ regulations require it, e.g. Tri-NAT assay.
Table 3.4

Pre-transplant investigations of the donor

Blood group and antibody screening

Coagulation studies

Complete blood count

Full/confirmatory HLA typing

Liver function tests

Urea and creatinine

Pregnancy test

Viral serology – Cytomegalovirus

 Epstein-Barr virus

 Hepatitis B surface antigen and core antibody

 Hepatitis C antigen

 HIV

 HTLV

 Treponemel screen

 Herpes simplex virus

 Varicella zoster virus

 Toxoplasma

Chest X-ray

Electrocardiogram

Under certain circumstances

Cytogenetic studies (chromosome fragility) if family history

Bone marrow examination

Echocardiogram or MUGA scan

Haemoglobin electrophoresis

Lung function tests

Haemoglobinopathy screen

3.5 Special Considerations

3.5.1 Screening of Elderly Donors

With more than 25% of HSCT now being performed in recipients >55 years of age, the chance of a higher age in matched sibling donors is also greater. This group of donors are more likely to have age-related medical conditions, and additional testing may be required to reduce the risk of donor-derived disease, e.g. transmission of an immune-mediated condition, e.g. asthma or psoriasis to the recipient, and reduce the risk to the donor. This includes PSA (prostate-specific antigen) in males, occult blood in stools, possible BM aspirate if results are abnormal, protein electrophoresis and CT chest if there is a history of smoking.

3.5.2 Screening of Paediatric Donors

Paediatric sibling donors are a unique underreported group with special challenges for the HSCT team and the family. Parents of the paediatric donor are in the difficult position of having to consent to both the donation and the transplant. JACIE and other professional bodies suggest the use of independent assessor and donor advocates in the case of paediatric donors to ensure the needs of the paediatric donors are met and that they are protected. Hutt et al. (2015) state that the intense experience of HSCT has a long-term impact on the whole family indicating the need for follow-up and psychological support. There can be a striking difference between the donors’ and parents’ view of the situation with the donor feeling a closer relationship with the recipient and also feeling responsible for them as well as the fact that the recipient owes them a debt of gratitude. Parents are concerned with two children and often feel that the donation process has a positive effect on family life not understanding any negative effect it may have on the donor feeling a pressure to donate or having that feeling of responsibility.

The needs of paediatric donor are sometimes left unmet since parents and healthcare professionals cannot always see the effect of the donation process on them. This can also be said to be the case in adult donors although they at least have life experience and knowledge which enables them to process and deal with their feelings in a way that a child often cannot.

3.5.3 Confidentiality

Information and care of the HSCT patients and their donor should be kept separate. Healthcare professionals must minimise their influence and that of the recipient and other family members which could complicate the potential donors’ decision to donate or not. Families are complex entities, and potential donors and recipients can be estranged or influenced, and donors can feel pressured to donate. A model of care which is independent to the recipient (i.e. independent medical assessment and counselling of the potential donor) increases the potential donors’ sense of security and allows for informed consent or refusal of donation. It is essential to separate the care of the donor from that of the recipient so that each individual can be focussed upon. The privacy of the donor must be respected and protected, and all potential donors should be given information at the time of the HLA typing about the potential process.

3.5.4 Donor Consent and Clearance

All donors should be reviewed and consented prior to the recipient commencing conditioning chemotherapy. They should be medically cleared and understand the implications if they withdraw their consent or participation once the recipient’s conditioning has commenced.

3.5.5 Stem Cell Source

While this is primarily dictated by the transplant medical assessment and the type of HSCT that the recipient is undergoing, the donor will also influence that decision. The donor has a choice in which type of donation method that they prefer, and both should be discussed. The donor may also have medical issues which influence the cell source, e.g. donors with significant back injuries or issues may not be suitable for bone marrow harvest, and unrelated donors who do not have adequate peripheral venous access may not be considered for apheresis due to the reluctance to insert a central access device in an unrelated donor.

Conclusion

Allogenic HSCT is a standard therapy in a number of malignant and non-malignant conditions. The choice of donor is a complex issue with far-reaching consequences both for the recipient and the donor.

Footnotes

  1. 1.

    Mendelian inheritance is where a person inherits two alleles, one from each parent. These alleles may be the same or different.

References

  1. Apperley J, Carreras E, Gluckman E, Masszi T. Haematopoeitic stem cell transplantation. 6th revised ed. 2012.Google Scholar
  2. Gragert L, et al. HLA match likelihoods for hematopoietic stem-cell grafts in the U.S. registry. N Engl J Med. 2014;371(4):339–48.CrossRefPubMedGoogle Scholar
  3. Hutt D, Nehari M, Munits-Shenkar D, Akalay Y, Toren A, Bielorai B. Haematopoietic stem cell donation: psychological perspectives of paediatric sibling donors and their parents. Bone Marrow Transplant. 2015;50:1–6.CrossRefGoogle Scholar
  4. Kisch, AM. Allogeneic stem cell transplant. Patient and sibling donors perspective. Malmo University. 2015.Google Scholar
  5. Kollman C, Howe CW, Ansetti C, et al. Donor characteristics as risk factors in recipients after transplantation of bone marrow from unrelated donors. Blood. 2001;98:2043–51.CrossRefPubMedGoogle Scholar
  6. Kulkarm S, Treleaven J. Patient selections: preliminary interview and screening of patient and donor. In: Treleaven J, Barrett AJ, editors. Haematopoietic stem cell transplantation in clinical practice. Churchill Livingstone: Elsevier; 2009.Google Scholar
  7. Rovira M, Mensa J, Carreras E, Infections in HSCT In: Apperley J, Carreras E, Gluckman E, Masszi T. The EBMT Handbook: Haematopoeitic stem cell transplantation. 6th revised ed. 2012.Google Scholar
  8. Shaw B. Human leukocyte antigen matching, compatibility testing and donor selection. In: Treleaven J, Barrett AJ, editors. Haematopoietic stem cell transplantation in clinical practice. Churchill Livingstone: Elsevier; Edinburgh 2009.Google Scholar

Copyright information

© EBMT and the Author(s) 2018

Open Access This chapter is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made. The images or other third party material in this book are included in the work's Creative Commons license, unless indicated otherwise in the credit line; if such material is not included in the work's Creative Commons license and the respective action is not permitted by statutory regulation, users will need to obtain permission from the license holder to duplicate, adapt or reproduce the material.

Authors and Affiliations

  1. 1.St James’s HospitalDublin 8Ireland

Personalised recommendations