Herpesviruses Infectious Diseases in Clinical Practice February 2018 - - PDF document

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Herpesviruses

Jennifer Babik, MD, PhD Associate Clinical Professor Division of Infectious Diseases, UCSF

Infectious Diseases in Clinical Practice February 2018

Learning Objectives

By the end of this talk, you will be able to:

• 1. Recognize the key clinical features of the most

common herpes virus infections.

• 1. Describe the important principles of diagnosis and

management of common herpes virus infections

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Roadmap

Case‐based approach to:

• HSV‐1
• HSV‐2 (non‐genital infections)
• VZV
• CMV
• EBV

Case #1

A 28 year old man presents with fever and severe sore throat after returning from his honeymoon. He has mild anterior cervical LAN and the oral exam shown. The rest of his exam is normal. Tests for Group A Strep, acute HIV, and EBV are negative.

Photo courtesy of Matt Russell.

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• 1. Throat swab for VZV DFA
• 1. Throat swab for HSV PCR
• 2. Throat swab for CMV PCR
• 3. Tonsillar biopsy to r/o lymphoma

The next best test is: Oral HSV: Primary Infection

• Children/young adults, HSV‐1
• Symptomatic in 10‐30%:
• Gingivostomatitis
• Pharyngitis/tonsillitis ‐ may not have vesicles!
• Systemic sx (can look like mono)
• Duration of symptoms 10‐14d
• Oral antivirals  duration of sx
• ACV 200mg PO 5x/day x 7 days
• Valacyclovir 1gm PO bid x 7 days

Ardino and Porter, J Oral Pathol Med 2008; 37:107. McMillan et al, Pediatr Infect Dis J 1993; 12:280. Ireland, Oxford Dictionary

• f Dentisty 2010. Cernik et al, Arch Intern Med 2008; 168:1137.

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Case #2

A 30 year old man presents to clinic complaining of “fever blisters” for the past 24 hours. He has moderate pain but mostly feels a great degree of stress and embarrassment about the lesions. This is his 5th episode in the last year.

Photo courtesy of Laura Pincus.

Oral antivirals

• 1. Shorten the time for lesions to heal
• 2. Are effective as suppressive therapy
• 3. Both #1 and #2
• 4. Have no treatment effect

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Recurrent Oral HSV: Herpes Labialis

• Almost always HSV‐1
• Recurrences in 20‐40% of HSV‐1 (+)
• 1.5 recurrences/year
• Triggers:
• Fever, URI
• UV light exposure (sun)
• Emotional stress, fatigue
• Immunosuppression
• Oral/facial surgery or trauma
• Menstruation

Cernik et al, Arch Intern Med 2008; 1168:1137. Ardino and Porter, J Oral Pathol Med 2008; 37:107.

Oral HSV Reactivation in Immunocompromised

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Test Sensitivity Specifcity Take home points

HSV: Diagnostics

Mosely et al, J Clin Microbiol 1981; 13:913. Wald et al, J Infect Dis 2003; 188:1345. Van Wagoner and Hook, Curr Infect Dis Rep 2012; 14:175. Lafferty et al, J Clin Microbiol 1987; 25:323.

PCR ~90% overall 99% Most sensitive test DFA Vesicle 70‐90% Ulcer 30% Crusted 10% 99% Rapid (hours) Slight  sensitivity c/w culture Culture Vesicle 70‐90% Ulcer 30‐40% Crusted 20‐30% 100% Moderate sensitivity Takes 1‐2 days

*Oral HSV is often a clinical diagnosis. May need to confirm if immunocompromised, severe, atypical, or not responding to Rx.

Oral HSV: Treatment

Episodic therapy

•  time to heal by 0.5‐2.5 days (does not abort lesions)
• Antivirals:
• Acyclovir 200mg PO 5x/day x 5 days
• Valacyclovir 2gm PO bid x 1 day

Suppressive therapy

•  recurrences by 40‐50% (if ≥4‐6 recurrences/year)
• Not known if can  oral HSV‐1 shedding or transmission
• Antivirals:
• Acyclovir 400mg PO bid
• Valacyclovir 500mg or 1000mg PO daily

Cernik et al, Arch Intern Med 2008; 168:1137.

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Oral HSV: Take Home Points

• Primary HSV‐1 can be a cause of pharyngitis in young

adults (and may not present with vesicles)

• HSV PCR of a lesion is the most sensitive diagnostic

test for mucocutaneous herpes infections

• Oral antivirals have a modest treatment effect: they

can shorten healing time and be used as suppressive therapy to prevent recurrences

Case #3

55 year old man is brought in by his neighbor for bizarre behavior for 12

• hours. He is found to be febrile and

has a witnessed seizure in the ED. MRI is shown. He is started on vancomycin, ceftriaxone, and acyclovir and is tapped 24 h later. Lumbar puncture:

• 50 WBC (89% lymphs), 50 RBC, protein 80, glucose 78
• CSF culture is NGTD
• PCR is negative for HSV and VZV

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What Would You Do With His Antibiotics?

• 1. Stop acyclovir
• 2. Change acyclovir to ganciclovir
• 3. Continue acyclovir

The HSV PCR May Be Negative Because:

• 1. He got 24 hours of acyclovir
• 2. It’s not a sensitive test
• 3. It’s early in the disease course

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HSV Encephalitis

• Epidemiology/Clinical:
• Accounts for 10‐20% of encephalitis
• >90% due to HSV‐1, most reactivation (HSV2 rare, in ICH)
• Fever, personality change, seizures, focal neuro findings
• CSF studies:
• WBCs: lymphocytic pleocytosis (median 130 cells)
• RBCs: elevated <500
• Mildly  protein (median 80 mg/dl), normal glucose

Whitley et al, JAMA 1982, 247:312. Whitley et al, JAMA 1989, 262:234. Tang et al, Clin Infect Dis 1999, 29:803. Domingues et al, Clin Infect Dis 1997, 25:86.

Can be normal in up to 15%

HSV Encephalitis: Diagnosis and Rx

• CSF PCR:
• 96% sensitive, 99% specific
• May have false (‐) in the first 3d  if suspicion is high re‐tap
• ACV has little effect on PCR (+) within the first 5 days of therapy
• MRI: temporal/frontal lobe involvement in 90%
• Treatment:
• ACV 10mg/kg IV q8h x 14‐21 days
• Can check HSV PCR at d14 to define duration

DeBiasi and Tyler, Clin Microbiol Rev 2004, 17:903. Tyler, Herpes 2004, 11 Suppl 2: 57A

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HSV Aseptic Meningitis

• 1st episode in primary genital HSV‐2 (women>men)
• Recurrences:
• 20‐30% of patients will have at least 1 recurrence
• Mollaret’s = repeated self‐limited episodes +/‐ skin lesions
• Antivirals needed?
• Consider ACV 10 mg/kg q8h or valacyclovir 1gm PO tid x 7‐

14d (some data for benefit in immunocompromised)

• Suppressive therapy not effective to prevent recurrences

Tyler, Herpes 2004, 11 Suppl 2: 57A. Aurelius et al, Clin Infect Dis 2012, 54: 1304. Berger and Houff, Arch Neurol 2008, 65:596. Noska et al, Clin Infect Dis 2015;60:237.

HSV Neuro Complications: Take‐Home

• HSV encephalitis is usually caused by HSV‐1 and

affects the frontal/temporal lobes

• CSF HSV PCR is very sensitive for HSV encephalitis:
• There can be false (‐) within the first 3 days of symptoms
• ACV has little effect on sensitivity within the first 5 days
• HSV meningitis is a complication of primary genital

herpes from HSV‐2 and can be recurrent

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Case #4

64 y/o man on prednisone 20mg/d for autoimmune hemolytic anemia presents with a painful progressive rash

• n his left leg in the L4 and L5

dermatomes. He is admitted with concern for disseminated zoster. Acyclovir is started but he still has new lesions on day 2

The Most Likely Diagnosis Is:

• 1. Disseminated zoster
• 2. Resistant zoster
• 3. Uncomplicated localized zoster
• 4. Herpetic whitlow

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Zoster: Key Clinical Features

• 80% have prodrome (lasts 2‐3 days)
• New vesicles appear for 2‐4 days

(antivirals  new lesions by 1‐2 days)

• Overlap into adjacent dermatomes in

20% (normal variation in innervation)

• PHN: pain lasting >3 months after

zoster episode, occurs in 10‐20%

Dworkin et al, Clin Infect Dis 2007; 44 (Suppl1): S1.

To confirm the dx, the most sensitive test is:

• 1. VZV DFA
• 2. VZV culture

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Test Sensitivity Specifcity Take home points

Cutaneous VZV: Diagnostics

Dworkin et al, CID 2007; 44 (Suppl1): S1. Helgason et al, Eur J Gen Pract 1996; 2:12. Kalman and Laskin, Am J Med 1986, 81:775.

PCR 95% 99% Most sensitive test Not always available DFA 90% 95% Rapid if in‐house (hours) Culture 60‐75% 100% Takes 1‐2 weeks to grow Usually not done

• Zoster is often a clinical diagnosis (~90% accurate).
• May need to confirm if immunocompromised, severe/disseminated

(e.g., hospitalized), atypical, or not responding to Rx.

Which is the Best Choice to  the Risk of PHN?

• 1. Prednisone
• 2. Valacyclovir
• 3. Valacyclovir and prednisone

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Zoster Treatment: Antivirals

• Benefits of therapy
•  duration new lesion formation by 1‐2 days
•  severity and duration of acute pain and rash
•  risk of PHN (inhibits viral replication, neural damage)
• Who to Treat?
• ≥50 years, mod‐severe pain/rash, immunocompromised
• Consider in all as benefit ( PHN) likely outweighs risk

Dworkin et al, Clin Infect Dis 2007; 44 (Suppl1): S1. Chen et al, Cochrane Database Syst Rev 2010; Issue 12.

Antiviral Options

• Drug options:
• Acyclovir 800 mg PO 5x/day, valacyclovir 1gm PO tid
• Duration 7‐10 days
• Immunocompromised: treat until all lesions crusted given

risk of relapse

• When to admit patients for IV acyclovir?
• Disseminated disease or CNS/eye complications
• Severely immunocompromised patients with localized

disease (to prevent dissemination)

• Consider in VZV ophthalmicus (V1 zoster)

Dworkin et al, Clin Infect Dis 2007; 44 (Suppl1): S1.

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Timing of Therapy

• Timing:
• All RCTs initiate therapy within 72 hours
• Starting at >72h hasn’t been well studied (?benefit up to 7d)
• If a patient presents at >72 hrs, would still treat if:
• Presence of new vesicles (indicates ongoing viral replication)
• Cutaneous, motor, ocular, neurologic complications
• Advanced age, severe pain (since these are risks for PHN)
• Immunocompromised
• V1 zoster (VZV ophthalmicus)

Dworkin et al, Clin Infect Dis 2007; 44 (Suppl1): S1.

Steroids in Acute Zoster

• 3 RCTs all show that addition of steroids to ACV:
• Accelerated healing, reduced pain, improved QOL
• But no decrease in PHN
• So when to consider steroids?
• Moderate to severe pain
• Facial nerve paralysis
• No contraindications to steroid use
• Regimen: Prednisone 60 mg/d then taper over 10‐21 d

Wood et al, N Eng J Med 1994; 330:896. Whitley et al, Annals Int Med 1996; 125:376. Esmann et al, Lancet 1987; 330:126. Chen et al, Cochrane Database Syst Rev 2010; Issue 12.

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Case #5

75 y/o man with well controlled HIV presents to clinic with a rash over his R eye in the V1 distribution associated with conjunctival injection.

How Would You Treat Him?

• 1. High dose PO valacyclovir and close follow‐up
• 2. Admission and IV acyclovir

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VZV Ophthalmicus

• Defined as zoster in the V1 distribution
• Without Rx, 50% will develop eye complications
• Conjunctivitis
• Anterior uveitis
• Necrotizing retinitis
• Keratitis
• Corneal ulcer
• Orbital apex syndrome

Harding et al, Br J Ophthalmol 1987.

VZV Ophthalmicus: Management

• Ophtho consult for those with:
• Eye symptoms
• Lesions on the tip or side of the nose
• Immunocompromised
• Antivirals:
• Treat all patients irrespective of duration
• f symptoms
• Intravenous ACV if immunocompromise
• r eye involvement

Dworkin et al, Clin Infect Dis 2007; 44 (Suppl1): S1

Hutchinson’s sign

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Case #6

A 59 year old man with SLE on cellcept and prednisone (10 mg/day) presents with diffuse vesicular rash. VZV DFA is positive and he is started on high dose acyclovir. He still has new lesions on HD#4.

What Would You Do?

• 1. Continue ACV and monitor for visceral involvement
• 2. Change to foscarnet given concern for resistance

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Disseminated VZV

• = lesions outside the primary or

adjacent dermatomes

• Usually immunocompromised,
• ccurs by viremic spread to skin
• Patients may have new lesions

for up to 2 weeks

• Patients are at high risk for

pneumonitis, hepatitis, DIC

Cohen, NEJM 2013, 369:255. Pergam et al, Am J Transplantation 2013.

Treatment

• Total duration 7‐14 days
• Use IV at least 7 days and

until all lesions are crusted

Another Complication of VZV: Encephalitis

• Usually occurs in immunocompromised patients
• Clinical:
• HA, fever, AMS, seizures
• Rash present in only 2/3 of cases
• CSF profile:
• Lymphocytic pleocytosis (median 110 cells/mm3)
• Elevated protein, glucose normal to slightly low
• Positive VZV PCR (sensitivity 80‐100%, specificity 98%)
• Positive VZV IgG (more sensitive than PCR, especially if chronic)
• Treatment: Acyclovir 10‐15 mg/kg IV q8 h for 10‐14 days

Gilden et al, NEJM 2000. Pahud et al, J Infect Dis 2011, 203:316. Tunkel et al, CID 2008, 47:303.

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Should This Patient Get the New Shingles Vaccine?

• 1. Yes
• 2. No
• 3. What new vaccine?

VZV Vaccines

Oxman et al, NEJM 2005. Lal et al, NEJM 2015.Cunningham et al, NEJM 2016.

Zostavax (ZVL) Shingrix (RZV) Type Live‐attenuated Recombinant # Doses One dose SC Two doses IM (2‐6 mo apart) Vaccine efficacy against zoster 70% (50‐59 years) 64% (60‐69 years) 38% (≥70 years) 97% (50‐59 years) 97% (60‐69 years) 90% (≥70 years) Vaccine efficacy against PHN 67% 89% Wanes over time? Yes , significant No or modest  (at 4 yr)

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New ACIP Recommendations (January 2018)

• Shingrix is now preferred over Zostavax
• Indications:
• All people ≥50 years old without contraindications
• Give even if a prior episode of zoster
• Give even if a prior dose of Zostavax (studied at 5 yrs afterward,

likely can given earlier)

• Don’t need to screen for prior varicella
• Contraindications:
• Allergy to the vaccine or its components
• Not yet studied in pregnancy

Dooling et al, MMWR 2018, 67:103. ACIP, January 2018.

Shingrix in Immunocompromised?

• Okay in “low dose immunosuppressive therapy”

(≤ 20mg/day prednisone of equivalent)

• What about other kinds of immunocompromise?
• These patients were excluded from the RCTs
• Phase I and II studies show it is safe
• Phase III efficacy studies underway – stay tuned!

Dooling et al, MMWR 2018, 67:103. ACIP, January 2018

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VZV: Take Home Points

• DFA or PCR are the diagnostic methods of choice for

cutaneous zoster

• Steroids provide no additional benefit to antivirals in 

risk of PHN

• Admit patients for IV acyclovir if they are severely

immunocompromised or have disseminated/CNS disease

• The recombinant zoster vaccine (Shingrix) is at least 90%

effective against zoster and PHN and is now the preferred zoster vaccine

Case #7

47 year old M with no PMH is admitted with fever and respiratory distress. CT shows prominent GGO. HIV Ab test is positive and CD4 is 56. BAL is performed and is positive for PCP. BAL is also positive for CMV

• culture. Plasma CMV PCR is

positive at 970 IU/mL.

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What Antibiotics Should You Start?

• 1. TMP‐SMX alone
• 2. TMP‐SMX plus ganciclovir
• 3. TMP‐SMX plus acyclovir
• 4. TMP‐SMX plus IVIG

Approach to CMV Infections

Immunocompetent Primary infection Asymptomatic or heterophile (‐) mononucleosis Diagnosis by serology Supportive Rx only

Navalpotro et al, J Clin Virol 2006; 35:193. Wreghitt et al, Clin Infect Dis 2003; 37:1603.

Immunocompromised Primary or reactivation

• Asymptomatic viremia
• CMV syndrome
• End‐organ disease

Diagnosis by tissue biopsy, blood PCR, culture Usually anti‐CMV therapy Define the Host

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Symptomatic CMV in Immunocompetent Patients

• Clinical: viral syndrome, abnormal LFTs
• Diagnosis (if testing is done):
• Positive CMV IgM
• Can be elevated for > 4‐12 mo after infection, during reactivation,
• r polyclonal stimulation (e.g. during acute EBV infection)
• Negative or low avidity IgG
• Treatment: supportive

Wreghitt et al, Clin Infect Dis 2003; 37:1603.

CMV Infection in Immunocompromised Patients

Asymptomatic Viremia Asymptomatic Plasma CMV PCR (+) Treatment depends

• n host

CMV Syndrome Fever plus bone marrow suppression (leukopenia and/or thrombocytopenia) Plasma CMV PCR (+) Treat all patients End‐Organ Disease

• Neuro: Encephalitis, Retinitis
• Pneumonitis
• GI: Colitis>Esophagitis
• Others: hepatitis, nephritis,

myocarditis, pancreatitis Plasma CMV PCR (+) (GI can be compartmentalized) Treat all patients

CMV Infection

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CMV in HIV+ Patients

• Asymptomatic viremia in up to 35% pts w/CD4<200
• Most common end‐organ disease:
• Retinitis
• GI (colitis > esophagitis)
• Pneumonitis is rare: BAL+ for CMV in ~50% of

patients (without CMV pneumonitis)

Durier et al, Clin Infect Dis 2013;57:147. Deayton et al, Lancet 2004; 363: 2116. Hayner et al, Chest 1995;107;735. Miles et al, Chest 1990;97;1072. CDC/NIH/HIVMA Guidelines for the prevention and treatment of OIs in HIV‐infected adults, 2015.

CMV End‐Organ Disease

CMV Colitis

• Fever, diarrhea (+/‐ bloody), abd pain
• Dx by colonoscopy with path, IHC
• Blood PCR can be negative

CMV Pneumonitis

• Fever, mild to severe resp failure
• CT shows diffuse bilateral GGO
• Dx by BAL: culture, path
• Blood PCR usually positive

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CMV Treatment

• IV vs PO?
• IV ganciclovir if severe, VL>1 million copies/mL, poor oral absorption
• PO valganciclovir okay for mild‐moderate disease
• IVIG?  Case‐by‐case basis for severe pneumonitis
• How long to treat?
• 2‐3 weeks and until PCR negative
• May consider secondary prophylaxis in selected patients
• PCR monitoring?
• Check 2 wks after starting therapy (viral load may actually  in 1st wk)
• Then check qweek until negative

Razonable et al, Am J Transplant 2013; 13:93. Asberg et al (VICTOR study group), Am J Transplant 2007; 7:2106.

Case #7 Continued

The patient was treated for PCP and started on ARVs. He was not treated for CMV. 3 weeks later he represents with fever but no other localizing signs or symptoms. Labs:

• WBC 1.0, platelets 81 (both previously normal)
• CMV viral load in the plasma is now 226,091 IU/mL.

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Review question: What is the diagnosis?

• 1. Asymptomatic CMV viremia
• 2. CMV syndrome
• 3. CMV end‐organ disease

CMV: Take‐Home Points

• Define your host: immunocompetent or

immunocompromised (HIV vs transplant/other)

• Determine which type of CMV infection your patient has:
• Asymptomatic viremia
• CMV syndrome
• End‐organ disease
• HIV+ patients are a special category:
• Commonly have asymptomatic viremia
• Can have severe end‐organ disease (retinitis, GI most common)
• Rarely have pneumonitis despite frequent +BAL for CMV

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Case #8

22 y/o woman presents with fever, sore throat, and cervical lymphadenopathy for 2 days. Heterophile antibody test is negative.

The Sensitivity of Heterophile Ab in 1st Week is:

• 1. 25%
• 2. 50%
• 3. 75%
• 4. >90%

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EBV

• 75% of US is seropositive by age 18
• Clinical:
• Incubation period 4‐6 weeks
• <18 y/o: Most are asymptomatic or nonspecific illness
• >18 y/o: Most are symptomatic
• Infectious mononucleosis = classic triad of sore throat,

cervical lymphadenopathy, fever

Balfour et al, J Infect Dis 2013; 207:80.

Diagnosis of IM: CBC with Differential

• Absolute lymph count > 4,000 x 106/L
• Sensitivity 84%
• Specificity 94%
• Atypical lymphs >10%
• Sensitivity 75%
• Specificity 92%

Luzuriaga and Sullivan, N Engl J Med 2010; 362:21. Vouloumanou et al, Curr Opin Hematol 2012; 19:14. Biggs et al, Laryngoscope 2013, 123:2401.

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Diagnosis of IM: Heterophile Antibody (Monospot)

Patient’s blood: IgM against viral antigens

+

Sheep or horse RBCs Agglutination X‐reactivity

• Sensitivity: 90‐95% after 1st week, but only 75% in the 1st week
• Specificity: 94%
• *No longer recommended by the CDC given false (+) and (–)*

Luzuriaga and Sullivan, N Engl J Med 2010; 362:21.

Diagnosis of IM: EBV Serologies

Luzuriaga and Sullivan, N Engl J Med 2010; 362:21.

IgM VCA IgG VCA IgG EBNA Acute Infection + +/− − Prior Infection − + +

• Sensitivity 85‐90%
• Specificity >95%

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Diagnosis of IM: EBV PCR

• Not a lot of data
• Positive early on, usually undetectable by week 3
• 2016 meta‐analysis of 4 small studies in kids/young

adults:

• Pooled sensitivity: 80%
• Pooled specificity: 95%
• May be helpful when other tests are inconclusive

Jiang et al, J Med Virol 2016; 88:871. Berth et al, J Clin Virol 2011; 50:184. Bauer et al, J Med Virol 2005; 75:54.

Mononucleosis: Treatment

• Steroids?  Not for all, maybe in select cases
• Cochrane review 2015: “insufficient evidence to the

efficacy of steroids for symptom control…lack of research

• n the side effects and long‐term complications”
• Consider short course to treat severe complications (e.g.,

upper‐airway obstruction)

• Antivirals?  NO, multiple RCTs show no benefit

Luzuriaga and Sullivan, N Engl J Med 2010; 362:21. Rezk et al, Cochrane Database Syst Rev 2015, issue 11. Balfour et al, J Clin Virol 2007; 39:16.

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Complications of EBV Infection

• Hematologic 25‐50%
• Hemolytic anemia
• Thrombocytopenia
• Aplastic anemia
• TTP/HUS
• DIC
• Trigger for HLH
• Splenic rupture

Luzuriaga and Sullivan, N Engl J Med 2010; 362:21.

• Neurologic 1‐5%
• Guillain–Barre syndrome
• Facial paralysis
• Aseptic meningitis
• Encephalitis
• Transverse myelitis
• Peripheral neuritis
• Optic neuritis

EBV Take Home Points

• Diagnosis of IM:
• Elevated ALC and atypical lymphs can be an important clue

to diagnosis

• Monospot testing is only 75% sensitive in the 1st week and

is no longer a recommended test

• Serology is 85‐90% sensitive
• PCR is positive early on with overall 80% sensitivity
• Treatment is supportive in most cases

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Thank You!

• Questions?