Bone Marrow Transplant Flashcards

1
Q

When host recogizes graft as foreign we get

A

rejection

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2
Q

When graft recognized host as foriegn this is

A

GVHD

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3
Q

T cells recognize:

A

histoINcompatability;

viruses, fungus, foreign substances

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4
Q

What must we do to a host so they don’t reject a graph?

A

Conditioning: ~7 day process

immune suppression to get rid of disease and host BM via chemotherapy

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5
Q

If you have lots of histoINcompatability you need______ conditioning during the conditioning phase

A

MORE

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6
Q

Why is prenatal screening so important?

A

We can find primary immune deficiencies right away and tx child before their immue system devos (don’t need conditioning)

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7
Q

Dr. Margolis referred to this as the ‘bane’ of a transplant doctors exsistance

A

Goals is working between GVH and GVL (graft vs leukemia) and we can’t separate those out yet

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8
Q

What type of cell is starting to be used more commonly instead of T cells in transplant?

A

NK cells

T cells cause GVHD

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9
Q

What type of cancer in a patient would BMT be an acceptable tx option in?

A
  • Patients with cancers that start in the bone marrow (Leukemia).
  • Patients with cancers that start elsewhere in the body (abdominal tumors, bone tumors).
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10
Q

What is the difference btwn autologous vs. allogeneic transplant

A
autologous = self 
allogeneic = non self or donor
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11
Q

What is the concept of an Auto Transplant?

A

its when you give pt back their own immune system or cells when they are going through chemotherapy so we can keep their chemo doses higher. (or if you have identical twin)

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12
Q

• Patients with bone marrow failure such as ______or hemoglobin abnormalities such as ______ and ______ can benefit from BMT

A

(aplastic anemia)

(thalassemia or sickle cell anemia).

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13
Q
  • Patients with primary immune deficiency syndromes_____

* Patients with other inborn errors of metabolism like_____ benefit from BMT

A

SCID

Hurlers

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14
Q

– Allogeneic Donor like an HLA matched sibling will likely have different:

A

Minor Histocompatibility antigens

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15
Q

if mom is your BMT match how close of a match is she?

A

1/2 HLA match

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16
Q

Order of increasing histoINcompatability

A

Autologous/identical twin –> matched sib –> unrelated donor –> Half matched paren

17
Q

Three sources of Hematopoietic Progenitor Cells

A
  • Bone Marrow (Gold standard)
  • Umbilical Cord Blood
  • Peripheral Blood
18
Q

Benefit of umbilical cord match?

A

– Lower risk of GVHD for same tissue match

19
Q

Why is Peripheral blood donation less desirable?

A

Peripheral Blood
– Higher risk of GVHD for same tissue match
– The HPC cells may be manipulated to remove cells:

20
Q

lower doses of chemotherapy and radiation, which are too low to eradicate all the bone marrow cells of a recipient. run lower risks of serious infections and transplant-related mortality while relying upon the graft versus tumor effect to resist the inherent increased risk of cancer relapse

A

Non-myeloablative conditioning

21
Q

given immediately prior to a transplant is called the conditioning regimen, the purpose of which is to help eradicate the patient’s disease prior to the infusion of HSC and to suppress immune reactions. The bone marrow can be ablated (destroyed) with dose-levels that cause minimal injury to other tissues. increases GVHD

A

Myeloablative conditioning

22
Q

Three steps of BMT

A

• Conditioning with chemotherapy+/- radiation
therapy.
– Different packages based on the variables ofdisease and donor.
– Myeloablative vs. Non myeloablative
• Infusion of the HPC product.
• Regrowth of the new marrow

23
Q

After BMT we are susceptible to bacteria because:

A
neutrophils are low, as well anytime
you have broken barriers due to mucositis and CVL
– Gram Positive
• Alpha Strep, Staph, Streps
– Gram Negative
• Hard to Kill Gram Negative Rods
– Anaerobes
• Clostridium Species
24
Q

What are we more susceptible to fungal infection post BMT?

A

When neutrophils are low, as well as when
one is on steroids
Moulds: Inhaled and angioinvasive (Aspergillus,Mucor)
• Sinus, Chest, Disseminated in skin
– Yeasts: Leave the GI/GU tract and disseminate
• Candida species

25
Q

How long are CD4 counts low post BMT and what does this make us concerned about?

A

Viral:
– Herpes Virus Family: Latency and reactivation
• HHV1,2; CMV; EBV; VZV; HHV6
– Community Acquired Virus follow community patterns:
• RSV, Influenza, Adenovirus, Enterovirus

26
Q

Late effects of BMT:

A
Second cancers, relapse, infertility
End-Organ Function
– Heart
– Lung
– Kidneys
– Liver
– Brain and Neurocognitive Development