CMV and Transplant Patients

What is CMV?

Human cytomegalovirus (CMV) is a type of virus. It is related to the virus that causes herpes. Like many other viruses, CMV can invade human cells. It can then use those cells to reproduce and spread. If the virus makes many copies of itself, it may disrupt how cells normally work.

In people with a normal immune system, CMV usually causes an illness similar to mononucleosis with sore throat, swollen lymph nodes, fatigue, and fever. However, your immune system keeps the virus in check so it can’t do any serious harm and the infection goes away by itself. Sometimes it doesn’t cause any symptoms. Very rarely, it can cause major problems in people with a normal immune system.

After infection, CMV often stays dormant in the body. That means that some of your cells stay infected with the virus. But the virus isn’t actively reproducing or causing symptoms. Sometimes the virus can become active again, especially in people who have weak immune systems. It then makes copies of itself and harms cells.

Infection with CMV is very common worldwide. Most people don’t even know they have it. In the U.S., infection rates are higher in women and older adults. It also more common in people from lower socioeconomic backgrounds.

What causes CMV in transplant patients?

CMV infection is spread from one person to another. The virus is passed on when a person comes into direct contact with an infected person’s bodily fluids. These include blood, urine, saliva, semen, tears, and breast milk. A pregnant mother can pass CMV to her unborn child.

People who have organ transplants are also more likely to get the virus. Transplants include a solid organ, bone marrow, or stem cell transplant. If you have had one of these, you must take medicine for life to prevent your immune system from damaging the donated tissue. Otherwise, the cells of the immune system may attack the transplanted organ. Your body thinks the new organ is a threat. This is called organ rejection.

The medicines you take after an organ transplant can help prevent damage to your donated organ. But they can have other effects on your immune system. They make it harder to fight off CMV and other infections.

Which transplant patients are at risk for CMV disease?

Certain types of transplants may have a higher risk for CMV. These include a lung or a small bowel transplant. You also might have a higher risk for the disease if you didn’t previously have the infection but your donor organ came from someone who had it.

You may also have a greater risk of CMV disease if your immune system is not working as it should. Your specific risk may depend on a number of factors, such as:

  • Your age
  • Other health problems you have
  • Whether you have had symptoms of transplant rejection
  • Specific medicines you are taking to prevent rejection

What are the symptoms of CMV in transplant patients?

An active CMV infection may cause a flu-like illness. Symptoms may include:

  • Fever
  • Chills
  • Fatigue
  • Muscle aches
  • Swollen lymph nodes

When CMV invades certain tissues, it can cause serious problems and even death. Most of the time, these symptoms start between 1 and 4 months after the transplant. They may start later if you were taking antiviral medicine at that time. They may also start after you stop taking this medicine.

How is CMV in transplant patients diagnosed?

Before your transplant, your healthcare provider may want to know whether you have an inactive infection with CMV. Your organ donor will also undergo testing for CMV. This information will help make a treatment plan to lower your chances of a CMV infection. A number of different tests might give this information. Your healthcare provider can let you know at this time if you or your organ donor have an inactive CMV infection.

If you don’t have a CMV infection, you might become newly infected with it if the donated organ was already carrying the virus. If you do have a CMV infection, there is a risk that the virus will reactivate after your transplant.

After your transplant, your healthcare provider may watch you for signs of active CMV infection. He or she will ask about any current symptoms and do a physical exam. You may also need other tests. These may include:

  • Basic blood work, to check your blood for signs of infection
  • Nucleic acid testing, to check for CMV infection
  • CMV pp65 antigen test, which quickly gives information about CMV infection status
  • Analysis of tissue samples under the microscope, to help confirm the disease

How is CMV in transplant patients treated?

If you have an active CMV infection that is causing symptoms, you will need treatment. Antiviral medicines like ganciclovir or valganciclovir can help. These medicines can help kill the virus. But they cannot make you completely virus free.

Based on how serious your illness is, you might take an antiviral medicine by mouth or through an IV. Your healthcare provider will watch your symptoms and the amount of virus in your body to decide the extent of your treatment. Healthcare providers don’t want to give these medicines for a long time. They can cause other side effects and problems.

Many people with active CMV infections often recover quite well, but sometimes an active sickness can cause severe problems. That’s especially the case if not treated early.

What are the complications of CMV in transplant patients?

An active CMV infection can cause major health problems, like:

  • Liver disease (hepatitis)
  • Lung infection (pneumonia)
  • Infection of the pancreas (pancreatitis)
  • Digestive disease (colitis)
  • Infection of the brain or spinal cord (meningitis or encephalitis)
  • Heart infection (myocarditis)
  • Blood clots in a vein (venous thrombosis)
  • Bacterial infection of the blood (bacteremia)

These health problems may cause other symptoms. They may also require their own treatments. Sometimes that may involve supportive care in an intensive care unit. These complications can even result in death.

Active CMV infection can also raise your risk for organ rejection. You may need another transplant. Preventive treatments have greatly reduced the number of people who have serious problems from active CMV infection.

CMV may also raise your risk for certain chronic disorders after the transplant. These include atherosclerosis and diabetes.

Can CMV in transplant patients be prevented?

Your healthcare team will do everything possible to help prevent active CMV infection. If your healthcare provider thinks you have a high risk for a new CMV infection or reactivation, he or she might start preventive antiviral medicines. You may take an antiviral medicine like valganciclovir right after your transplant. You may need to stay on it for some months. The medicine will greatly lower your chance of getting an active CMV infection. But sometimes people get an active CMV infection after stopping these medicines.

Other times, your healthcare provider might try to prevent you from having the symptoms of the infection using something called preemptive therapy. In this case, your healthcare provider might want you to have weekly lab tests to see if CMV has become active. In this way, he or she can find an active infection before you have any symptoms. It allows quicker treatment. That will cut your chance of complications.

When should I call my healthcare provider?

Call your healthcare provider right away if you have any symptoms of a possible active CMV infection. These include:

  • Fever and chills
  • Fatigue
  • Nausea and vomiting
  • Shortness of breath
  • Chest pain

Key points about CMV and transplant patients

  • CMV is a virus. It only rarely causes problems in people with a normal immune system. In transplant patients, the virus can cause major problems.
  • After your transplant, the CMV virus may reactivate. Or you might get a new infection. Both of these can cause symptoms of active CMV disease.
  • An active CMV infection can raise the chance of organ rejection.
  • Your healthcare provider may try to prevent an active CMV infection by giving you antiviral medicines.

Next steps

Tips to help you get the most from a visit to your healthcare provider:

  • Know the reason for your visit and what you want to happen.
  • Before your visit, write down questions you want answered.
  • Bring someone with you to help you ask questions and remember what your provider tells you.
  • At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you.
  • Know why a new medicine or treatment is prescribed, and how it will help you. Also know what the side effects are.
  • Ask if your condition can be treated in other ways.
  • Know why a test or procedure is recommended and what the results could mean.
  • Know what to expect if you do not take the medicine or have the test or procedure.
  • If you have a follow-up appointment, write down the date, time, and purpose for that visit.
  • Know how you can contact your provider if you have questions.
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