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 Table of Contents  
REVIEW ARTICLE
Year : 2014  |  Volume : 1  |  Issue : 2  |  Page : 39-44

Rabies: An overview


Department of Clinical Hematology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India

Date of Web Publication29-Dec-2014

Correspondence Address:
Tarun Kumar Dutta
Department of Clinical Hematology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry - 605 006
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2349-4220.147998

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  Abstract 

Rabies is a fatal disease caused by rabies virus, a neurotropic virus and a prototype of Lyssavirus of Rhabdoviridae family. It is transmitted to human beings through infected saliva of dogs and cats during bite. Dog is the cause of more than 90% of human rabies in India. The incubation period is 4-8 weeks (but it may vary from 5 days to 7 years). There are two clinical types of rabies - encephalitic (furious) and paralytic (dumb) types. In the encephalitic (furious) form, the principal malfunction is in the brain stem and limbic system. Patient has hydrophobia in the full-blown form, but the mind remains clear till the end. Death occurs within a week after the onset of symptoms. Paralytic rabies resembles Guillain-Barre syndrome. Diagnosis is mostly clinical. However, direct fluorescent antibody test is used to identify the antigen in skin biopsy from the nape of neck. In the postmortem specimen, demonstration of Negri bodies in the brain confirms the diagnosis. Anti-rabies vaccine is used for pre- and post-exposure prophylaxis. The commonly used intramuscular (IM) regimen is being superseded by intradermal (ID) vaccine because it makes the treatment economical. Whereas touching of animal or lick on intact skin does not require vaccination, any transdermal bite with bleeding requires immediate administration of rabies immunoglobulin (RIG) and simultaneous vaccination with a tissue culture vaccine (TCV). Minor abrasion without bleeding may require only vaccination and no RIG. Rabies human monoclonal antibody (RMAb) is the newest entry in the prophylaxis of rabies which may ultimately replace RIG. Prognosis is grave since there are just six reports of survivors. Treatment is mainly palliative with heavy sedation and/or therapeutic coma (Milwaukee protocol).

Keywords: Intradermal vaccine, intramuscular vaccine, post-exposure prophylaxis, pre-exposure prophylaxis, rabies


How to cite this article:
Dutta TK. Rabies: An overview. Int J Adv Med Health Res 2014;1:39-44

How to cite this URL:
Dutta TK. Rabies: An overview. Int J Adv Med Health Res [serial online] 2014 [cited 2018 Aug 16];1:39-44. Available from: http://www.ijamhrjournal.org/text.asp?2014/1/2/39/147998


  introduction Top


Rabies is a fatal disease of nearly worldwide distribution that is caused by a filterable neurotropic virus present in the saliva of the infected animals and transmitted to humans through their infected saliva.

Urban rabies is propagated chiefly by unimmunized domestic or street dogs and cats. Street virus is the natural virus present in rabid animals. Wild-life or sylvatic-type rabies is propagated by wolves, foxes, skunks, jackals, etc., which are the main reservoirs and transmitters of rabies. [1] These animals maintain a cycle among them and transmit the disease to dogs and domestic animals. Humans may contract rabies by intrusion into the wild-life cycle of rabies. Bat rabies occurs in certain Latin American countries where the vampire bat serves as an important host and vector for rabies. In the USA, insectivorous bats and wild animals are the most important vectors at present.

The source of infection in humans is the saliva of rabid animals. Domestic dog is the cause of more than 90% of human rabies in India. Dogs also infect cats and other domestic species.

Rabies-free countries are Australia, New Zealand, Japan, Taiwan, Hong Kong, Singapore, Fiji, UK, Ireland, Norway, Sweden, Jamaica, and Barbados. In India, the islands of Andaman and Lakshadweep are rabies free.


  Epidemiology Top


The true incidence is unknown. In India, the estimated mortality is 25,000 to 50,000 deaths per year. Recent figures in China show less than 1000 cases per year. In Bangladesh, about 2000 deaths and in Nepal, about 200 deaths occur per year. Only 0.01% cases of human rabies occur in the temperate zones.


  Aetiopathogenesis Top


Rabies virus is the prototype of the genus Lyssavirus of the large family of Rhabdoviridae. It is a bullet-shaped virus containing a single-strand of ribonucleic acid (RNA) combined with nucleoprotein that forms a helical coil. The virus is rapidly inactivated by heat. At 56°C, the half-life is less than 1 min. The lipid coat is disrupted by 1% soap solution.

Humans are infected by inoculation of virus-laden saliva by the bite of a rabid dog or animal. Licking on abraded skin or mucus membrane may also result in infection. Scratching by claws can also cause infection. The virus cannot enter through intact skin.

The rabies virus travels in the nerves and is carried centripetally by the flow of axoplasm to the dorsal root ganglion. It multiplies further in the dorsal root ganglion and causes characteristic prodromal symptoms and paresthesias at the site of inoculation. From there it travels to the brain, where massive viral replication occurs. Then the virus migrates along the efferent nerves to almost every organ such as adrenal medulla, cornea, pancreas, nerve twiglet of the hair follicle, and salivary gland, and this leads to virus shedding in the saliva. Virus may also be shed in milk and urine.

At autopsy, widespread infection is usually found in the brain, particularly in the brainstem, hippocampus, and basal ganglia. Congestion of blood vessels of the central nervous system (CNS) and petechial hemorrhages of the pia-arachnoid are found. Histological examination shows perivascular cellular infiltration of lymph spaces. Negri bodies can be detected within the cytoplasm of nerve cells as round or oval eosinophilic inclusion bodies, particularly in the hippocampus and Purkinje cells of the cerebellum. Negri bodies are also found in the brain of more than 95% of rabid animals. [1]


  Clinical Features Top


Incubation period is usually 4-8 weeks, but may vary from 5 days to 7 years. Face, neck, and head bites which are close to the CNS have a shorter incubation period.

It may be of two types:

  • Encephalitic type (furious rabies) - observed in the majority of cases
  • Paralytic type (dumb rabies) - observed in about 20% of cases


Encephalitic type (furious rabies)

The onset is usually sudden. But prodromal symptoms are noted for 2-3 days before the hydrophobic syndrome appears. Only a proportion of people bitten by a rabid animal develop the disease, but once manifested, the disease is almost invariably fatal. Specific prodromal features include paresthesias and itching over the healed bite wound scar. Other features are fever, headache, tachycardia, anxiety, insomnia, restlessness, and myalgias. After 2-3 days, the stage of excitement supervenes. There is mental excitement, restlessness, hyperesthesia, and hydrophobia. Hyodrophobia consists of sudden spasm of muscles of the mouth, pharynx, larynx, and the whole of the respiratory musculature, particularly the diaphragm and muscles of inspiration. The attack can be induced by offering water to patients. As the glass of water approaches the mouth, typical spasmodic jerks with violent contraction of diaphragm and other inspiratory muscles occur and water is ejected from the mouth. Afterward, the sight and even the sound of water may provoke the distressing spasm. In the later stage, a wide number of stimuli like sudden sound, strong lights, and even the suggestion of water may induce the attack. Cold air or blowing of air due to fan may also induce an attack (aerophobia). The mind remains clear during the intervals. Hallucinations, delusions accompanied by biting, mania, and spitting may develop later. There is malfunction of brain stem, limbic system, and higher centers.

Death occurs within a week after the onset of symptoms.

Paralytic type (dumb rabies)

It characteristically occurs in bat-transmitted rabies. It also occurs in partially vaccinated persons. Patient presents with flaccid paralysis. It resembles Guillain-Barre syndrome. [2] The stage of excitement is absent. In a few days, paralysis may ascend to involve the respiratory muscles. There is fever and profuse sweating.

The patient has a comparatively longer survival.


  Diagnosis Top


Diagnosis is confirmed by virus isolation, identification of antigen, and detection of antibodies. [3] Virus culture is positive in the first week from saliva, throat swab, eye swab, and cerebrospinal fluid (CSF).

Antigen detection

Direct fluorescent antibody test is used to identify the antigen in skin biopsies taken from the nape of the neck, where hair follicles are highly innervated. It is a sensitive test and positive results are found in 60-100% cases. The corneal smear test is not so sensitive and false-positive results occur.

Antibody detection

Seroconversion occurs during the second week of illness in unvaccinated patients. Antirabies antibody detection in serum and CSF confirms the diagnosis.

Negri body detection

The offending animal is captured (if possible) and humanely killed for demonstration of Negri bodies in the brain. Fluorescent antigen can also be detected in the animal's brain, and confirms the diagnosis of rabies.


  Differential diagnosis Top


This includes other causes of encephalitis or bulbar paralysis (including post-vaccinal encephalomyelitis), Guillain-Barre syndrome, and hysterical pseudorabies.


  Treatment Top


Once symptoms develop, only palliative treatment is possible. Seizures should be controlled by heavy sedation. Diazepam 10 mg, six hourly, supplemented by chlorpromazine 50 mg, if necessary, can be used to control seizures. Fluid balance and nutrition must be maintained by intravenous route. Airway and oxygenation should be maintained. On rare occasions, partially immunized patients survive due to extensive intensive care. To date, there are six survivors of rabies including one 6-year-old girl from India, the majority with some neurological sequelae. Induced coma (Milwaukee protocol) has been found useful in some cases.

Milwaukee protocol [4]

In September, a 15-year-old girl developed features of rabies 37 days after being bitten by a bat on her finger. In an attempt to treat the patient, doctors placed her on induced coma and gave ketamine, midazolam, ribavarin, and amantadine. After 31 days of intensive care, the patient recovered, but had some neurological deficits like inability to walk and maintain balance. She became the first case of rabies who survived without being vaccinated.

This original Milwaukee protocol has undergone several modifications and out of 25 patients thus treated, only 2 have survived.


  Prophylaxis Top


Rabies vaccine can be used for pre-exposure prophylaxis (PrEP) as well as post-exposure prophylaxis (PEP). The commonly used regimen of intramuscular (IM) administration (1 ml) of vaccine is being superseded by intradermal (ID) vaccination, which requires lesser quantity of vaccine (0.1 ml) and is equally effective. [5]

Post-exposure prophylaxis

PEP is begun immediately after an exposure. Before initiating anti-rabies treatment, one should establish the category of the animal bite [Table 1]. This categorization helps in deciding the future course of action. [3] In addition, tetanus toxoid and proper antibiotics should be used.
Table 1: WHO classification of wounds

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PEP consists of a regimen of one dose of immunoglobulin (passive immunization) and five doses of rabies vaccine over a period of 28 days. Vaccines should be given intramuscularly. Alternatively, vaccine can be given intradermally also. Human rabies immunoglobulin (RIG) should be infiltrated around the wound and any remaining portion should be administered intramuscularly, preferably in the gluteal region. Alternatively, equine immunoglobulin 40 IU/kg may be administered. Equine immunoglobulin is cheaper, but the incidence of serum reactions is more.

IM regimen

There are currently four types of vaccines available, and the regimen most commonly used in India for IM administration is described below:

Vaccines

  1. Tissue culture vaccines
    1. Human diploid cell vaccine (HDCV): One dose - 1 ml (IM)
    2. Purified chick embryo cell vaccine (PCECV): One dose - 1 ml (IM)
    3. Purified Vero cell rabies vaccine (PVRV): One dose - 0.5 ml (IM)
  2. Purified duck embryo vaccine (Vaxirab): One dose - 1 ml (IM)

    Regimen: Essen schedule (standard WHO five-dose IM regimen) - The course for PEP should consist of IM administration of five injections on days 0, 3, 7, 14, and 28.




Human rabies immunoglobulin (20 IU/kg)

The sixth dose is optional and given to individuals who are immune deficient. Day 0 indicates the date of first injection.

Vaccines are ideally given in the deltoid region, and may be given in antero-lateral part of the thigh for children.

ID regimen

ID recommendation by WHO is a newer attempt to have effective antibody titers against rabies with a lower total requirement of vaccine. The principle that allows ID vaccination to be effective at a lower dose is that it may be due to the better response to an equal volume of antigen which is placed in contact with Langerhans cells of the epidermis and because of multiple sites of vaccination at the same time to obtain maximum drainage of antigen-presenting cells to the lymph nodes.

On the basis of the recommendations on ID administration of rabies vaccine by WHO and reports of safety, efficacy, and feasibility trials conducted in India, the Drug Controller General of India (DCGI) approved the use of reduced dose ID vaccination in 2006.

The following vaccines are currently approved by DCGI for use by ID route:

Vaccines

PVRV -

Verorab, Aventis Pasteur (Sanofi Pasteur India Pvt. Ltd.)

PCECV - Rabipur, Chiron Behring Vaccines Pvt. Ltd.

PVRV - Pasteur Institute of India, Coonoor, India

PVRV - Abhayrab, Human Biologicals Institute

DCGI has recommended the updated Thai Red Cross 2-2-2-0-2 schedule of ID vaccination, which is as follows:



This involves injection of only 0.1 ml of reconstituted vaccine per ID site and the vaccination has to be given at two different sites on a single visit (one on each deltoid area, an inch above the insertion of deltoid muscle) on days 0, 3, 7, and 28, using a 1-ml insulin syringe. A bleb formed after injection is a sign of successful ID administration. It is best used in anti-rabies clinics for group vaccinations (for a minimum of 10 persons at a time) because the contents of a broken ampoule of 1 ml have to be used within 8 h and the requirement for a single person on a single visit will be just 0.2 ml and the rest will thus go waste.

ID vaccination is not indicated in patients with immunocompromised states or those on immunosuppressants like chloroquine or prednisolone. They should take full dose of IM injections.

Wound treatment

Wound treatment is the most important part of treatment and should begin immediately. It minimizes the viral load. Wound should be thoroughly cleaned with soap and water. Povidone iodine or 70% alcohol should be used to irrigate the wound. Suturing of the wound is to be avoided. Bites of rats, mice, rabbits, and guinea pigs do not require anti-rabies PEP.

Pre-exposure prophylaxis

PrEP is recommended for animal handlers and laboratory workers dealing with rabies virus. PrEP consists of three doses of rabies vaccine given either intramuscularly or intradermally on days 0, 7, and 21.


  Prognosis Top


The prognosis of rabies encephalomyelitis is grave. At the time of the bite, before the virus has invaded the nervous system, correct and prompt cleansing of the wound and proper post-exposure immunization reduce the risk of development of rabies from 50% to less than 5%. The risk is highest following head bites. Interposition of clothing, extent of tissue laceration, and immediate local treatment modify the prognosis.


  Recent advances Top


  1. It has been now possible to achieve active immunization with four doses of tissue culture vaccine (instead of five). [6]
  2. Fully human monoclonal antibodies (mAbs) have been found to be safer and equally efficacious than conventional RIG. [7],[8] Currently, only human and equine polyclonal anti-rabies immunoglobulin (HRIG and ERIG) are available. Replacement of HRIG and ERIG with a safer and more widely available product is recommended. Recently, a combination of two human MAbs, CR57 and CR4098, that has high potential has been identified. A head-to-head comparison between CR57/CR4098 MAb cocktail and HRIG has been made. The MAb cocktail neutralized all viruses from a panel of 26 representative street rabies virus isolates. In combination with the vaccine, the MAb cocktail protected Syrian hamsters against lethal rabies when administered 24 h after exposure, comparable with the results obtained with HRIG. Furthermore, the MAb cocktail did not interfere with rabies vaccine differently from HRIG. These results demonstrated that the human MAb cocktail of CR57 and CR4098 is a safe and efficacious alternative to RIG in rabies PEP. [9]

    In a phase 1 trial at the King Edward Memorial Hospital (KEM) in Mumbai, India, 74 healthy volunteers were randomized into several groups that either received rabies human monoclonal antibody (RMAb) or hRIG combined with vaccine. Results showed that the RMAb was well tolerated by all subjects, with no serious side effects. A dose of RMAb produced similar level of rabies virus neutralizing antibody in the blood from volunteers who received RMAb and vaccine as compared to those who received the standard regimen of hRIG and vaccine. Based on these data, Serum Institute of India has received approval to conduct the current trial. [10]
  3. Sudarshan et al. have found more compliant "new 1 week ID regimen" equally effective as the conventional 4 week ID regimen. Patients in this trial received PCECV or PVRV at four sites on days 0, 3, and 7 (4-44). [11]


 
  References Top

1.
Cook GC, Zumla AI, editors. Manson's Tropical Diseases. 22 nd ed. London: Saunders Elsevier; 2009. p. 799-814.   Back to cited text no. 1
    
2.
Dutta TK, Ghotekar LH, Sahoo RK. Rabies - an update. In: Gupta SB, editor. API Medicine Update. Mumbai: The Association of Physicians of India; 2005. p. 680-3.  Back to cited text no. 2
    
3.
WHO Expert Consultation on Rabies. WHO Technical Report Series 931. Geneva: World Health Organization; 2005.   Back to cited text no. 3
    
4.
Willoughby RE Jr, Tieves KS, Hoffman GM, Ghanayem NS, Amlie-Lefond CM, Schwabe MJ, et al. Survival after treatment of rabies with induction of coma. N Engl J Med 2005;352:2508-14.  Back to cited text no. 4
    
5.
National Guidelines for Rabies Prophylaxis and Intra-dermal Administration of Cell Culture Rabies Vaccines, 2007. National Institute of Communicable Diseases, Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India, New Delhi.   Back to cited text no. 5
    
6.
Rupprecht CE, Briggs D, Brown CM, Franka R, Katz SL, Kerr HD, et al.; Centers for Disease Control and Prevention (CDC). Use of a reduced (4-dose) vaccine schedule for postexposure prophylaxis to prevent human rabies: Recommendations of the advisory committee on immunization practices. MMWR Recomm Rep 2010;59:1-9.  Back to cited text no. 6
    
7.
Nagarajan T, Rupprecht CE, Dessain SK, Rangarajan PN, Thiagarajan D, Srinivasan VA. Human monoclonal antibody and vaccine approaches to prevent human rabies. Curr Top Microbiol Immunol 2008;317:67-101.  Back to cited text no. 7
    
8.
de Kruif J, Bakker AB, Marissen WE, Kramer RA, Throsby M, Rupprecht CE, et al. A human monoclonal antibody cocktail as a novel component of rabies postexposure prophylaxis. Annu Rev Med 2007;58:359-68.  Back to cited text no. 8
    
9.
Goudsmit J, Marissen WE, Weldon WC, Niezgoda M, Hanlon CA, Rice AB, et al. Comparison of an anti-rabies human monoclonal antibody combination with human polyclonal anti-rabies immune globulin. J Infect Dis 2006;193:796-801.  Back to cited text no. 9
    
10.
Shelton ML. Clinical trial for rabies monoclonal antibody. UMass Medical, Serum Institute of India Partner on Pivotal Trial. Public release date: 2012 Aug 7.  Back to cited text no. 10
    
11.
Sudarshan MK, Narayana DH, Madhusudana SN, Holla R, Ashwin BY, Gangaboraiah B, et al . Evaluation of a one week intradermal regimen for rabies post-exposure prophylaxis: Results of a randomized, open label, active-controlled trial in healthy adult volunteers in India. Hum Vaccin Immunother 2012;8:1077-81.  Back to cited text no. 11
    



 
 
    Tables

  [Table 1]


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introduction
Epidemiology
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