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TRANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09
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Page 1: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

TRANSPLANTATIONJunior Basic Science

Carla Fisher, MD

12-15-09

Page 2: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

TRANSPLANT IMMUNOLOGY

Major antigens responsible for rejection are the genes known as the major histocompatibility complex (MHC)

In humans MHC is known as human leukocyte antigen (HLA) Class I (-A, -B, -C) are found on all nucleated cells Class II (-DR, -DP, -DQ) are expressed on antigen

presenting cells (B lymphocytes, monocytes, dendritic cells)

Can get humoral or cellular (more common) rejection

Page 3: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

TRANSPLANT IMMUNOLOGY

Allorecognition recognition of foreign HLA molecules by recipient

T cells

Panel reactive antibody (PRA) Detects presence of donor-specific antibodies by

testing reactivity of the recipient’s serum to a panel of common A, B, and DR antigens

Results expressed as a percentage Higher PRA indicates patient more likely to have

an episode of acute cellular rejection

Page 4: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

IMMUNOSUPPRESSION

Induction: administered immediately post operatively to induce immunosuppression (biologic)

Maintenance: to maintain immunosuppression once recovered from OR (non-biologic)

In 1960s, 2 drugs were available. Currently there are 15+ available.

Page 5: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

IMMUNOSUPPRESSION

CORTICOSTEROIDS historically first used proven benefits however many side effects, esp in long

term for this reason steroids have been removed from many

newer immunosuppressive protocols first line therapy for acute rejection common side effects:

mild cushingoid facies and habitus acne increased appetite mood changes htn prox muscle weakness glucose intolerance poor wound healing

Page 6: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

IMMUNOSUPPRESSION

AZATHIOPRINE (IMURAN) inhibits purine synthesis which inhibits T cells 6-mercaptopurine is active metabolite side effect is myelosuppression

MYCOPHENALATE MOFETIL similar to azathioprine as an anti-metabolite but

is more selective

Page 7: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

IMMUNOSUPPRESSION CYCLOSPORINE

binds cyclophilllin and inhibits genes for cytokine synthesis (IL-2) decreases T cell activation

calcineurin inhibitor side effects include nephrotoxicity, hepatotoxicity,

tremors, seizures, hirsuitism

TACROLIMUS (FK-506, Prograf) actions similar to CSA but much more potent calcineurin inhibitor similar SEs to CSA but more GI and neurologic

changes

SIROLIMUS does not affect calcineurin activity

Page 8: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

BIOLOGIC IMMUNOSUPPRESSION

ANTITHYMOCYTE GLOBULIN (ATGAM) equine polyclonal antibodies directed against

antigens on T cells must be infused via central line, premedication

with steroids/benadryl induction therapy

THYMOGLOBULIN rabbit polyclonal antibodies similar to ATGAM, may be more effective

Page 9: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

MONOCLONAL ANTIBODY IMMUNOSUPPRESSION

used for prevention and treatment of acute (severe) rejection

Muromonab-CD3 anti-CD25 mAbs (basiliximab and daclizumab) humanized anti-CD52 mAb alemtuzumab

(Campath-1H) anti-CD20 (rituximab) anti–lymphocyte function-associated antigen-1

(anti–LFA-1) anti–intercellular adhesion molecule-1 (anti–

ICAM-1) anti–tumor necrosis factor alpha (TNF-α)

(infliximab)

Page 10: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

TYPES OF REJECTION Hyperacute:

occurs within minutes caused by preformed abs that should be picked

up by crossmatch Accelerated acute:

occurs within first few days cellular and antibody mediated response caused by sensitized T cells to donor antigens

Acute: less common with modern immunosuppression within days to months after transplantation predominantly a cell mediated process,

lymphocytes usually manifested with abnormal laboratory

values but pt asymptomatic Chronic:

months to years after transplant increasingly common problem multifactorial

Page 11: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

WHICH OF THE FOLLOWING STATEMENTS REGARDING KIDNEY TRANSPLANTATION IS/ARE TRUE?

A. The one year actuarial survival rate for all patients is greater than 95%

B. The survival rate following transplantation appears to be improved only in diabetic patients

C. The primary cause of graft loss after 5 years is chronic rejection

D. Treatment of chronic refection has improved significantly over the past 10 years

E. Treatment of renal failure with transplantation becomes cost effective at the end of the second transplant year

Page 12: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

KIDNEY TRANSPLANTATION currently approx 70,000 patients awaiting

kidney transplant mortality usually related to stroke/MI attach to iliac vessels, usually on the R post op UOP impt to assess graft (must know

pre operative UOP) decreased UOP post kidney transplant?

hypovolemia vascular thrombosis bladder outlet obstruction ureter obstruction drug toxicity acute rejection

Page 13: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

KIDNEY TRANSPLANTATION - COMPLICATIONS

Urologic can be due to poor blood supply to ureter drainage and stenting usually 1st line treatment

Vascular complications renal artery (1%) or vein thrombosis renal artery stenosis

Lymphocele incidence 0.6% -18%

Rejection Usually represented by ↑ Cr w/u includes US and biopsy 5 year graft survival 65% cadaveric, 75% living

Page 14: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

ALLOCATION OF CADAVERIC RENAL ALLOGRAFTS IS DEPENDENT ON WHICH OF THE FOLLOWING?

A. Time on hemodialysisB. HLA compatibilityC. Recipient’s ageD. PRA resultsE. Region of transplant center

Page 15: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

PANCREAS TRANSPLANTATION

commonly done simultaneously with kidney tx

do pancreas tx alone when pt’s diabetes severe enough to warrant immunosuppression

need donor celiac, SMA, portal vein

Page 16: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

PANCREAS/KIDNEY TRANSPLANTATION

Successful tx results in: Stabilization of retinopathy ↓ neuropathy ↑ nerve conduction velocity ↓ autonomic dysfunction (gastroparesis) ↓ orthostatic hypotension

No reversal of vascular disease

Page 17: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

PANCREAS TRANSPLANTATION - COMPLICATIONS

*common Thrombosis (6%) Hemorrhage Infection Pancreatitis Rejection

Page 18: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

ISLET CELL TRANSPLANTATION

Utilizes islets of Langerhans Still requires immunosuppression In 1995, a report of the International Islet

Transplant Registry indicated that of 270 recipients, only 5% were insulin independent at 1 year posttransplant.

Page 19: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

LIVER TRANSPLANTATION

Used for acute and chronic liver disease Hepatitis (most common indication) ETOH (must be abstinent x 6 mos) Primary biliary cirrhosis, primary sclerosing

cholangitis Biliary atresia Hepatocellular CA

Single tumor < 5cm Up to 3 tumors < 3cm

APACHE score – best predictor of 1 year survival

Model for End stage Liver Disease

Page 20: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

LIVER TRANSPLANTATION – POSTOPERATIVE CARE

Serial laboratory check Coags Bilirubin Glucose LFTs

Page 21: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

LIVER TRANSPLANTATION - COMPLICATIONS

Bile leak (#1) – PTC, stent Primary nonfunction – requires

retransplantation Hepatic artery thrombosis Abscesses IVC stenosis cholangitis

Page 22: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

REGARDING LIVER TX FOR PATIENTS CHRONICALLY INFECTED WITH HEPATITIS C VIRUS, WHICH OF THE FOLLOWING STATEMENTS IS/ARE TRUE?A. Post-transplant re-infection with hepatitis C

virus occurs in all patientsB. Post-transplant re-infection with hepatitis C

virus can be prevented with combination therapy with interferon and ribavirin and hyperimmunoglobulin

C. Post-transplant re-infection with hepatitis C virus causes cirrhosis in approximately 30% of patients at 5 years after liver transplantation

D. The clinical course of hepatitis C after re-infection is more virulent than that of the original infection

Page 23: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

INFECTIONS

Bacterial More likely to occur immediately post transplant Prevention of pneumocystis pneumonia with

Bactrim Viral

CMV Fungal

Mortality 20%

Page 24: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

WHICH OF THE FOLLOWING STATEMENTS IS/ARE TRUE REGARDING CMV INFECTION?

A. infection with CMV following kidney transplantation is the strongest predictor of poor long-term survival

B. The incidence of symptomatic CMV infection is declining owing to the utilization of screening tests

C. Patients at highest risk for developing CMV infection are those who test seropositive for CMV IgG

D. CMV infection is more likely to cause chronic allograft nephropathy than infection with BK virus

E. CMV infection can be indistinguishable from acute EBV infection

Page 25: T RANSPLANTATION Junior Basic Science Carla Fisher, MD 12-15-09.

MALIGNANCY

Non-melanomatous skin cancers – 3-7x more likely

Post transplant lymphoproliferative disorder – 2-3x more likely EBV

Gynecologic/urologic cancers Kaposi’s sarcoma